Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.44372308G>A | CA290942658 | ITGA2B | c.*56C>T (n.*56C>T) c.2490C>T c.369C>T c.153C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372308G>C | CA2638213407 | ITGA2B | c.*56C>G (n.*56C>G) c.2490C>G c.369C>G c.153C>G | gnomAD v4 |
17 | g.44372308G= | CA2261364313 | ITGA2B | c.*56C= (n.*56C=) c.2490C= c.369C= c.153C= | |
17 | g.44372311del | CA2638213406 | ITGA2B | c.*56del (n.*56del) c.2490del c.369del c.153del | gnomAD v4 |
17 | g.44372309G>C | CA2638213410 | ITGA2B | c.*55C>G (n.*55C>G) c.2489C>G c.368C>G c.152C>G | gnomAD v4 |
17 | g.44372309G= | CA2261364314 | ITGA2B | c.*55C= (n.*55C=) c.2489C= c.368C= c.152C= | |
17 | g.44372309G>T | CA2261364315 | ITGA2B | c.*55C>A (n.*55C>A) c.2489C>A c.368C>A c.152C>A | dbSNP |
17 | g.44372312C= | CA2261364316 | ITGA2B | c.*52G= (n.*52G=) c.2486G= c.365G= c.149G= | |
17 | g.44372312C>T | CA290942661 | ITGA2B | c.*52G>A (n.*52G>A) c.2486G>A c.365G>A c.149G>A | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372313G>A | CA8602442 | ITGA2B | c.*51C>T (n.*51C>T) c.2485C>T c.364C>T c.148C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372313G= | CA2261364318 | ITGA2B | c.*51C= (n.*51C=) c.2485C= c.364C= c.148C= | |
17 | g.44372313G>T | CA2261364317 | ITGA2B | c.*51C>A (n.*51C>A) c.2485C>A c.364C>A c.148C>A | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372314G>A | CA2809589671 | ITGA2B | c.*50C>T (n.*50C>T) c.2484C>T c.363C>T c.147C>T | |
17 | g.44372314G>C | CA2638213415 | ITGA2B | c.*50C>G (n.*50C>G) c.2484C>G c.363C>G c.147C>G | gnomAD v4 |
17 | g.44372314G>T | CA2638213416 | ITGA2B | c.*50C>A (n.*50C>A) c.2484C>A c.363C>A c.147C>A | gnomAD v4 |
17 | g.44372316del | CA2638213417 | ITGA2B | c.*48del (n.*48del) c.2482del c.361del c.145del | gnomAD v4 |
17 | g.44372316G>A | CA2638213418 | ITGA2B | c.*48C>T (n.*48C>T) c.2482C>T c.361C>T c.145C>T | gnomAD v4 |
17 | g.44372317C= | CA2261364319 | ITGA2B | c.*47G= (n.*47G=) c.2481G= c.360G= c.144G= | |
17 | g.44372317C>T | CA8602443 | ITGA2B | c.*47G>A (n.*47G>A) c.2481G>A c.360G>A c.144G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372318A= | CA2261364320 | ITGA2B | c.*46T= (n.*46T=) c.2480T= c.359T= c.143T= | |
17 | g.44372318A>C | CA2261364321 | ITGA2B | c.*46T>G (n.*46T>G) c.2480T>G c.359T>G c.143T>G | dbSNP gnomAD v4 |
17 | g.44372320G>A | CA8602444 | ITGA2B | c.*44C>T (n.*44C>T) c.2478C>T c.357C>T c.141C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372320G= | CA2261364322 | ITGA2B | c.*44C= (n.*44C=) c.2478C= c.357C= c.141C= | |
17 | g.44372321T>G | CA2261364324 | ITGA2B | c.*43A>C (n.*43A>C) c.2477A>C c.356A>C c.140A>C | dbSNP gnomAD v4 |
17 | g.44372321T= | CA2261364323 | ITGA2B | c.*43A= (n.*43A=) c.2477A= c.356A= c.140A= | |
17 | g.44372323G>T | CA2638213423 | ITGA2B | c.*41C>A (n.*41C>A) c.2475C>A c.354C>A c.138C>A | gnomAD v4 |
17 | g.44372324C>T | CA2733742463 | ITGA2B | c.*40G>A (n.*40G>A) c.2474G>A c.353G>A c.137G>A | dbSNP |
17 | g.44372325A>C | CA2638213424 | ITGA2B | c.*39T>G (n.*39T>G) c.2473T>G c.352T>G c.136T>G | gnomAD v4 |
17 | g.44372325A>G | CA2638213425 | ITGA2B | c.*39T>C (n.*39T>C) c.2473T>C c.352T>C c.136T>C | gnomAD v4 |
17 | g.44372326C= | CA2261364325 | ITGA2B | c.*38G= (n.*38G=) c.2472G= c.351G= c.135G= | |
17 | g.44372326C>G | CA2809589676 | ITGA2B | c.*38G>C (n.*38G>C) c.2472G>C c.351G>C c.135G>C | |
17 | g.44372326C>T | CA8602445 | ITGA2B | c.*38G>A (n.*38G>A) c.2472G>A c.351G>A c.135G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372327G>A | CA8602446 | ITGA2B | c.*37C>T (n.*37C>T) c.2471C>T c.350C>T c.134C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372327G= | CA2261364326 | ITGA2B | c.*37C= (n.*37C=) c.2471C= c.350C= c.134C= | |
17 | g.44372327G>T | CA2261364327 | ITGA2B | c.*37C>A (n.*37C>A) c.2471C>A c.350C>A c.134C>A | dbSNP gnomAD v4 |
17 | g.44372327_44372328insA | CA656365619 | ITGA2B | c.*36_*37insT (n.*36_*37insT) c.2470_2471insT c.349_350insT c.133_134insT | |
17 | g.44372328C>T | CA2638213430 | ITGA2B | c.*36G>A (n.*36G>A) c.2470G>A c.349G>A c.133G>A | gnomAD v4 |
17 | g.44372330C>G | CA2638213431 | ITGA2B | c.*34G>C (n.*34G>C) c.2468G>C c.347G>C c.131G>C | gnomAD v4 |
17 | g.44372332A= | CA2261364329 | ITGA2B | c.*32T= (n.*32T=) c.2466T= c.345T= c.129T= | |
17 | g.44372332A>C | CA2261364328 | ITGA2B | c.*32T>G (n.*32T>G) c.2466T>G c.345T>G c.129T>G | dbSNP |
17 | g.44372332A>G | CA8602447 | ITGA2B | c.*32T>C (n.*32T>C) c.2466T>C c.345T>C c.129T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372333C>A | CA2638213435 | ITGA2B | c.*31G>T (n.*31G>T) c.2465G>T c.344G>T c.128G>T | gnomAD v4 |
17 | g.44372333C>T | CA2809589677 | ITGA2B | c.*31G>A (n.*31G>A) c.2465G>A c.344G>A c.128G>A | |
17 | g.44372334C= | CA2261364330 | ITGA2B | c.*30G= (n.*30G=) c.2464G= c.343G= c.127G= | |
17 | g.44372334C>T | CA290942693 | ITGA2B | c.*30G>A (n.*30G>A) c.2464G>A c.343G>A c.127G>A | dbSNP |
17 | g.44372335C= | CA2261364331 | ITGA2B | c.*29G= (n.*29G=) c.2463G= c.342G= c.126G= | |
17 | g.44372335C>T | CA8602448 | ITGA2B | c.*29G>A (n.*29G>A) c.2463G>A c.342G>A c.126G>A | dbSNP ExAC |
17 | g.44372336T>C | CA2638213437 | ITGA2B | c.*28A>G (n.*28A>G) c.2462A>G c.341A>G c.125A>G | gnomAD v4 |
17 | g.44372337C>T | CA2638213438 | ITGA2B | c.*27G>A (n.*27G>A) c.2461G>A c.340G>A c.124G>A | gnomAD v4 |
17 | g.44372338C= | CA2261364332 | ITGA2B | c.*26G= (n.*26G=) c.2460G= c.339G= c.123G= | |
17 | g.44372338C>G | CA290942711 | ITGA2B | c.*26G>C (n.*26G>C) c.2460G>C c.339G>C c.123G>C | dbSNP |
17 | g.44372338C>T | CA2261364333 | ITGA2B | c.*26G>A (n.*26G>A) c.2460G>A c.339G>A c.123G>A | dbSNP |
17 | g.44372339T= | CA2261364334 | ITGA2B | c.*25A= (n.*25A=) c.2459A= c.338A= c.122A= | |
17 | g.44372340dup | CA772284485 | ITGA2B | c.*24dup (n.*24dup) c.2458dup c.337dup c.121dup | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372343A= | CA2261364335 | ITGA2B | c.*21T= (n.*21T=) c.2455T= c.334T= c.118T= | |
17 | g.44372343A>G | CA983994058 | ITGA2B | c.*21T>C (n.*21T>C) c.2455T>C c.334T>C c.118T>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372346A= | CA2261364336 | ITGA2B | c.*18T= (n.*18T=) c.2452T= c.331T= c.115T= | |
17 | g.44372346A>G | CA8602449 | ITGA2B | c.*18T>C (n.*18T>C) c.2452T>C c.331T>C c.115T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372347T>G | CA2547600405 | ITGA2B | c.*17A>C (n.*17A>C) c.2451A>C c.330A>C c.114A>C | gnomAD v4 |
17 | g.44372349G>A | CA2638213447 | ITGA2B | c.*15C>T (n.*15C>T) c.2449C>T c.328C>T c.112C>T | gnomAD v4 |
17 | g.44372349G>C | CA772284489 | ITGA2B | c.*15C>G (n.*15C>G) c.2449C>G c.328C>G c.112C>G | dbSNP |
17 | g.44372349G= | CA2261364337 | ITGA2B | c.*15C= (n.*15C=) c.2449C= c.328C= c.112C= | |
17 | g.44372350T>C | CA8602450 | ITGA2B | c.*14A>G (n.*14A>G) c.2448A>G c.327A>G c.111A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372350T= | CA2261364338 | ITGA2B | c.*14A= (n.*14A=) c.2448A= c.327A= c.111A= | |
17 | g.44372351G>A | CA626118978 | ITGA2B | c.*13C>T (n.*13C>T) c.2447C>T c.326C>T c.110C>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372351G= | CA2261364339 | ITGA2B | c.*13C= (n.*13C=) c.2447C= c.326C= c.110C= | |
17 | g.44372352T>C | CA2576290830 | ITGA2B | c.*12A>G (n.*12A>G) c.2446A>G c.325A>G c.109A>G | |
17 | g.44372355G>A | CA772284497 | ITGA2B | c.*9C>T (n.*9C>T) c.2443C>T c.322C>T c.106C>T | dbSNP gnomAD v4 |
17 | g.44372355G= | CA2261364340 | ITGA2B | c.*9C= (n.*9C=) c.2443C= c.322C= c.106C= | |
17 | g.44372356C>T | CA2638213451 | ITGA2B | c.*8G>A (n.*8G>A) c.2442G>A c.321G>A c.105G>A | gnomAD v4 |
17 | g.44372359C= | CA2261364341 | ITGA2B | c.*5G= (n.*5G=) c.2439G= c.318G= c.102G= | |
17 | g.44372359C>T | CA2261364342 | ITGA2B | c.*5G>A (n.*5G>A) c.2439G>A c.318G>A c.102G>A | dbSNP |
17 | g.44372360A>G | CA2638213452 | ITGA2B | c.*4T>C (n.*4T>C) c.2438T>C c.317T>C c.101T>C | gnomAD v4 |
17 | g.44372362C= | CA2261364343 | ITGA2B | c.*2G= (n.*2G=) c.2436G= c.315G= c.99G= | |
17 | g.44372362C>T | CA2261364344 | ITGA2B | c.*2G>A (n.*2G>A) c.2436G>A c.315G>A c.99G>A | dbSNP |
17 | g.44372363A>G | CA2638213453 | ITGA2B | c.*1T>C (n.*1T>C) c.2435T>C c.314T>C c.98T>C | gnomAD v4 |
17 | g.44372364T>A | CA399787559 | ITGA2B | c.3120A>T (p.Ter1040Cys) c.2434A>T c.313A>T c.97A>T c.3018A>T (p.Ter1006Cys) c.3003A>T (p.Ter1001Cys) | |
17 | g.44372364T>C | CA399787561 | ITGA2B | c.3120A>G (p.Ter1040Trp) c.2434A>G c.313A>G c.97A>G c.3018A>G (p.Ter1006Trp) c.3003A>G (p.Ter1001Trp) | |
17 | g.44372364T>G | CA399787564 | ITGA2B | c.3120A>C (p.Ter1040Cys) c.2434A>C c.313A>C c.97A>C c.3018A>C (p.Ter1006Cys) c.3003A>C (p.Ter1001Cys) | |
17 | g.44372364T= | CA2261364345 | ITGA2B | c.3120A= (p.Ter1040=) c.2434A= c.313A= c.97A= c.3018A= (p.Ter1006=) c.3003A= (p.Ter1001=) | |
17 | g.44372365C>A | CA399787566 | ITGA2B | c.3119G>T (p.Ter1040Leu) c.2433G>T c.312G>T c.96G>T c.3017G>T (p.Ter1006Leu) c.3002G>T (p.Ter1001Leu) | |
17 | g.44372365C>G | CA399787569 | ITGA2B | c.3119G>C (p.Ter1040Ser) c.2433G>C c.312G>C c.96G>C c.3017G>C (p.Ter1006Ser) c.3002G>C (p.Ter1001Ser) | |
17 | g.44372365C>T | CA500260508 | ITGA2B | c.3119G>A (p.Ter1040=) c.2433G>A c.312G>A c.96G>A c.3017G>A (p.Ter1006=) c.3002G>A (p.Ter1001=) | |
17 | g.44372366_44372370dup | CA915940262 | ITGA2B | c.3115_3119dup (p.Ter1040TrpextTer?) c.2429_2433dup c.308_312dup c.92_96dup c.3013_3017dup (p.Ter1006TrpextTer?) c.2998_3002dup (p.Ter1001TrpextTer?) | ClinVar dbSNP |
17 | g.44372366A= | CA2261364346 | ITGA2B | c.3118T= (p.Ter1040=) c.2432T= c.311T= c.95T= c.3016T= (p.Ter1006=) c.3001T= (p.Ter1001=) | |
17 | g.44372366A>C | CA399787576 | ITGA2B | c.3118T>G (p.Ter1040Gly) c.2432T>G c.311T>G c.95T>G c.3016T>G (p.Ter1006Gly) c.3001T>G (p.Ter1001Gly) | dbSNP |
17 | g.44372366A>G | CA399787574 | ITGA2B | c.3118T>C (p.Ter1040Arg) c.2432T>C c.311T>C c.95T>C c.3016T>C (p.Ter1006Arg) c.3001T>C (p.Ter1001Arg) | gnomAD v4 |
17 | g.44372366A>T | CA399787572 | ITGA2B | c.3118T>A (p.Ter1040Arg) c.2432T>A c.311T>A c.95T>A c.3016T>A (p.Ter1006Arg) c.3001T>A (p.Ter1001Arg) | |
17 | g.44372367C>A | CA399787582 | ITGA2B | c.3117G>T (p.Glu1039Asp) c.2431G>T c.310G>T c.94G>T c.3015G>T (p.Glu1005Asp) c.3000G>T (p.Glu1000Asp) | |
17 | g.44372367C= | CA2261364347 | ITGA2B | c.3117G= (p.Glu1039=) c.2431G= c.310G= c.94G= c.3015G= (p.Glu1005=) c.3000G= (p.Glu1000=) | |
17 | g.44372367C>G | CA399787579 | ITGA2B | c.3117G>C (p.Glu1039Asp) c.2431G>C c.310G>C c.94G>C c.3015G>C (p.Glu1005Asp) c.3000G>C (p.Glu1000Asp) | |
17 | g.44372367C>T | CA500260512 | ITGA2B | c.3117G>A (p.Glu1039=) c.2431G>A c.310G>A c.94G>A c.3015G>A (p.Glu1005=) c.3000G>A (p.Glu1000=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372368T>A | CA399787588 | ITGA2B | c.3116A>T (p.Glu1039Val) c.2430A>T c.309A>T c.93A>T c.3014A>T (p.Glu1005Val) c.2999A>T (p.Glu1000Val) | |
17 | g.44372368T>C | CA399787591 | ITGA2B | c.3116A>G (p.Glu1039Gly) c.2430A>G c.309A>G c.93A>G c.3014A>G (p.Glu1005Gly) c.2999A>G (p.Glu1000Gly) | |
17 | g.44372368T>G | CA399787594 | ITGA2B | c.3116A>C (p.Glu1039Ala) c.2430A>C c.309A>C c.93A>C c.3014A>C (p.Glu1005Ala) c.2999A>C (p.Glu1000Ala) | |
17 | g.44372369C>A | CA399787596 | ITGA2B | c.3115G>T (p.Glu1039Ter) c.2429G>T c.308G>T c.92G>T c.3013G>T (p.Glu1005Ter) c.2998G>T (p.Glu1000Ter) | |
17 | g.44372369C>G | CA399787598 | ITGA2B | c.3115G>C (p.Glu1039Gln) c.2429G>C c.308G>C c.92G>C c.3013G>C (p.Glu1005Gln) c.2998G>C (p.Glu1000Gln) | |
17 | g.44372369C>T | CA399787601 | ITGA2B | c.3115G>A (p.Glu1039Lys) c.2429G>A c.308G>A c.92G>A c.3013G>A (p.Glu1005Lys) c.2998G>A (p.Glu1000Lys) | COSMIC |
17 | g.44372370C>A | CA500260520 | ITGA2B | c.3114G>T (p.Gly1038=) c.2428G>T c.307G>T c.91G>T c.3012G>T (p.Gly1004=) c.2997G>T (p.Gly999=) | |
17 | g.44372370C>G | CA500260534 | ITGA2B | c.3114G>C (p.Gly1038=) c.2428G>C c.307G>C c.91G>C c.3012G>C (p.Gly1004=) c.2997G>C (p.Gly999=) | gnomAD v4 |
17 | g.44372370C>T | CA500260536 | ITGA2B | c.3114G>A (p.Gly1038=) c.2428G>A c.307G>A c.91G>A c.3012G>A (p.Gly1004=) c.2997G>A (p.Gly999=) | dbSNP |
17 | g.44372371C>A | CA399787616 | ITGA2B | c.3113G>T (p.Gly1038Val) c.2427G>T c.306G>T c.90G>T c.3011G>T (p.Gly1004Val) c.2996G>T (p.Gly999Val) | |
17 | g.44372371C>G | CA399787619 | ITGA2B | c.3113G>C (p.Gly1038Ala) c.2427G>C c.306G>C c.90G>C c.3011G>C (p.Gly1004Ala) c.2996G>C (p.Gly999Ala) | |
17 | g.44372371C>T | CA399787622 | ITGA2B | c.3113G>A (p.Gly1038Glu) c.2427G>A c.306G>A c.90G>A c.3011G>A (p.Gly1004Glu) c.2996G>A (p.Gly999Glu) | gnomAD v4 |
17 | g.44372372C>A | CA399787627 | ITGA2B | c.3112G>T (p.Gly1038Trp) c.2426G>T c.305G>T c.89G>T c.3010G>T (p.Gly1004Trp) c.2995G>T (p.Gly999Trp) | |
17 | g.44372372C= | CA2261364348 | ITGA2B | c.3112G= (p.Gly1038=) c.2426G= c.305G= c.89G= c.3010G= (p.Gly1004=) c.2995G= (p.Gly999=) | |
17 | g.44372372C>G | CA399787629 | ITGA2B | c.3112G>C (p.Gly1038Arg) c.2426G>C c.305G>C c.89G>C c.3010G>C (p.Gly1004Arg) c.2995G>C (p.Gly999Arg) | gnomAD v4 |
17 | g.44372372C>T | CA399787630 | ITGA2B | c.3112G>A (p.Gly1038Arg) c.2426G>A c.305G>A c.89G>A c.3010G>A (p.Gly1004Arg) c.2995G>A (p.Gly999Arg) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.44372373C>A | CA8602452 | ITGA2B | c.3111G>T (p.Glu1037Asp) c.2425G>T c.304G>T c.88G>T c.3009G>T (p.Glu1003Asp) c.2994G>T (p.Glu998Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372373C= | CA2261364349 | ITGA2B | c.3111G= (p.Glu1037=) c.2425G= c.304G= c.88G= c.3009G= (p.Glu1003=) c.2994G= (p.Glu998=) | |
17 | g.44372373C>G | CA290942765 | ITGA2B | c.3111G>C (p.Glu1037Asp) c.2425G>C c.304G>C c.88G>C c.3009G>C (p.Glu1003Asp) c.2994G>C (p.Glu998Asp) | dbSNP gnomAD v4 |
17 | g.44372373C>T | CA500260554 | ITGA2B | c.3111G>A (p.Glu1037=) c.2425G>A c.304G>A c.88G>A c.3009G>A (p.Glu1003=) c.2994G>A (p.Glu998=) | |
17 | g.44372373_44372376delinsCTCT | CA2261364350 | ITGA2B | c.3108_3111delinsAGAG (p.Glu1036=) c.2422_2425delinsAGAG c.301_304delinsAGAG c.85_88delinsAGAG c.3006_3009delinsAGAG (p.Glu1002=) c.2991_2994delinsAGAG (p.Glu997=) | |
17 | g.44372374T>A | CA399787635 | ITGA2B | c.3110A>T (p.Glu1037Val) c.2424A>T c.303A>T c.87A>T c.3008A>T (p.Glu1003Val) c.2993A>T (p.Glu998Val) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372374T>C | CA8602453 | ITGA2B | c.3110A>G (p.Glu1037Gly) c.2424A>G c.303A>G c.87A>G c.3008A>G (p.Glu1003Gly) c.2993A>G (p.Glu998Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372374T>G | CA399787640 | ITGA2B | c.3110A>C (p.Glu1037Ala) c.2424A>C c.303A>C c.87A>C c.3008A>C (p.Glu1003Ala) c.2993A>C (p.Glu998Ala) | |
17 | g.44372374T= | CA2261364351 | ITGA2B | c.3110A= (p.Glu1037=) c.2424A= c.303A= c.87A= c.3008A= (p.Glu1003=) c.2993A= (p.Glu998=) | |
17 | g.44372376_44372378del | CA8602451 | ITGA2B | c.3108_3110del (p.Glu1037del) c.2422_2424del c.301_303del c.85_87del c.3006_3008del (p.Glu1003del) c.2991_2993del (p.Glu998del) | dbSNP ExAC |
17 | g.44372375C>A | CA399787646 | ITGA2B | c.3109G>T (p.Glu1037Ter) c.2423G>T c.302G>T c.86G>T c.3007G>T (p.Glu1003Ter) c.2992G>T (p.Glu998Ter) | |
17 | g.44372375C>G | CA399787650 | ITGA2B | c.3109G>C (p.Glu1037Gln) c.2423G>C c.302G>C c.86G>C c.3007G>C (p.Glu1003Gln) c.2992G>C (p.Glu998Gln) | |
17 | g.44372375C>T | CA399787651 | ITGA2B | c.3109G>A (p.Glu1037Lys) c.2423G>A c.302G>A c.86G>A c.3007G>A (p.Glu1003Lys) c.2992G>A (p.Glu998Lys) | COSMIC |
17 | g.44372376T>A | CA399787654 | ITGA2B | c.3108A>T (p.Glu1036Asp) c.2422A>T c.301A>T c.85A>T c.3006A>T (p.Glu1002Asp) c.2991A>T (p.Glu997Asp) | |
17 | g.44372376T>C | CA500260566 | ITGA2B | c.3108A>G (p.Glu1036=) c.2422A>G c.301A>G c.85A>G c.3006A>G (p.Glu1002=) c.2991A>G (p.Glu997=) | |
17 | g.44372376T>G | CA399787656 | ITGA2B | c.3108A>C (p.Glu1036Asp) c.2422A>C c.301A>C c.85A>C c.3006A>C (p.Glu1002Asp) c.2991A>C (p.Glu997Asp) | |
17 | g.44372376_44372379delinsTTCA | CA2261364352 | ITGA2B | c.3105_3108delinsTGAA (p.Asp1035=) c.2419_2422delinsTGAA c.298_301delinsTGAA c.82_85delinsTGAA c.3003_3006delinsTGAA (p.Asp1001=) c.2988_2991delinsTGAA (p.Asp996=) | |
17 | g.44372377T>A | CA399787661 | ITGA2B | c.3107A>T (p.Glu1036Val) c.2421A>T c.300A>T c.84A>T c.3005A>T (p.Glu1002Val) c.2990A>T (p.Glu997Val) | |
17 | g.44372377T>C | CA399787663 | ITGA2B | c.3107A>G (p.Glu1036Gly) c.2421A>G c.300A>G c.84A>G c.3005A>G (p.Glu1002Gly) c.2990A>G (p.Glu997Gly) | |
17 | g.44372377T>G | CA399787664 | ITGA2B | c.3107A>C (p.Glu1036Ala) c.2421A>C c.300A>C c.84A>C c.3005A>C (p.Glu1002Ala) c.2990A>C (p.Glu997Ala) | |
17 | g.44372382_44372384del | CA8602454 | ITGA2B | c.3105_3107del (p.Asp1035del) c.2419_2421del c.298_300del c.82_84del c.3003_3005del (p.Asp1001del) c.2988_2990del (p.Asp996del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372378C>A | CA399787669 | ITGA2B | c.3106G>T (p.Glu1036Ter) c.2420G>T c.299G>T c.83G>T c.3004G>T (p.Glu1002Ter) c.2989G>T (p.Glu997Ter) | |
17 | g.44372378C>G | CA399787670 | ITGA2B | c.3106G>C (p.Glu1036Gln) c.2420G>C c.299G>C c.83G>C c.3004G>C (p.Glu1002Gln) c.2989G>C (p.Glu997Gln) | |
17 | g.44372378C>T | CA399787668 | ITGA2B | c.3106G>A (p.Glu1036Lys) c.2420G>A c.299G>A c.83G>A c.3004G>A (p.Glu1002Lys) c.2989G>A (p.Glu997Lys) | gnomAD v4 |
17 | g.44372379A= | CA2261364353 | ITGA2B | c.3105T= (p.Asp1035=) c.2419T= c.298T= c.82T= c.3003T= (p.Asp1001=) c.2988T= (p.Asp996=) | |
17 | g.44372379A>C | CA399787672 | ITGA2B | c.3105T>G (p.Asp1035Glu) c.2419T>G c.298T>G c.82T>G c.3003T>G (p.Asp1001Glu) c.2988T>G (p.Asp996Glu) | |
17 | g.44372379A>G | CA500260588 | ITGA2B | c.3105T>C (p.Asp1035=) c.2419T>C c.298T>C c.82T>C c.3003T>C (p.Asp1001=) c.2988T>C (p.Asp996=) | |
17 | g.44372379A>T | CA399787674 | ITGA2B | c.3105T>A (p.Asp1035Glu) c.2419T>A c.298T>A c.82T>A c.3003T>A (p.Asp1001Glu) c.2988T>A (p.Asp996Glu) | dbSNP gnomAD v4 |
17 | g.44372380T>A | CA399787678 | ITGA2B | c.3104A>T (p.Asp1035Val) c.2418A>T c.297A>T c.81A>T c.3002A>T (p.Asp1001Val) c.2987A>T (p.Asp996Val) | |
17 | g.44372380T>C | CA399787681 | ITGA2B | c.3104A>G (p.Asp1035Gly) c.2418A>G c.297A>G c.81A>G c.3002A>G (p.Asp1001Gly) c.2987A>G (p.Asp996Gly) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372380T>G | CA399787684 | ITGA2B | c.3104A>C (p.Asp1035Ala) c.2418A>C c.297A>C c.81A>C c.3002A>C (p.Asp1001Ala) c.2987A>C (p.Asp996Ala) | |
17 | g.44372380T= | CA2261364354 | ITGA2B | c.3104A= (p.Asp1035=) c.2418A= c.297A= c.81A= c.3002A= (p.Asp1001=) c.2987A= (p.Asp996=) | |
17 | g.44372381C>A | CA399787687 | ITGA2B | c.3103G>T (p.Asp1035Tyr) c.2417G>T c.296G>T c.80G>T c.3001G>T (p.Asp1001Tyr) c.2986G>T (p.Asp996Tyr) | |
17 | g.44372381C>G | CA399787690 | ITGA2B | c.3103G>C (p.Asp1035His) c.2417G>C c.296G>C c.80G>C c.3001G>C (p.Asp1001His) c.2986G>C (p.Asp996His) | |
17 | g.44372381C>T | CA399787693 | ITGA2B | c.3103G>A (p.Asp1035Asn) c.2417G>A c.296G>A c.80G>A c.3001G>A (p.Asp1001Asn) c.2986G>A (p.Asp996Asn) | |
17 | g.44372382A>C | CA399787696 | ITGA2B | c.3102T>G (p.Asp1034Glu) c.2416T>G c.295T>G c.79T>G c.3000T>G (p.Asp1000Glu) c.2985T>G (p.Asp995Glu) | |
17 | g.44372382A>G | CA500260618 | ITGA2B | c.3102T>C (p.Asp1034=) c.2416T>C c.295T>C c.79T>C c.3000T>C (p.Asp1000=) c.2985T>C (p.Asp995=) | |
17 | g.44372382A>T | CA399787701 | ITGA2B | c.3102T>A (p.Asp1034Glu) c.2416T>A c.295T>A c.79T>A c.3000T>A (p.Asp1000Glu) c.2985T>A (p.Asp995Glu) | |
17 | g.44372382_44372385delinsATCT | CA2261364355 | ITGA2B | c.3099_3102delinsAGAT (p.Glu1033=) c.2413_2416delinsAGAT c.292_295delinsAGAT c.76_79delinsAGAT c.2997_3000delinsAGAT (p.Glu999=) c.2982_2985delinsAGAT (p.Glu994=) | |
17 | g.44372383T>A | CA399787704 | ITGA2B | c.3101A>T (p.Asp1034Val) c.2415A>T c.294A>T c.78A>T c.2999A>T (p.Asp1000Val) c.2984A>T (p.Asp995Val) | ClinVar |
17 | g.44372383T>C | CA399787706 | ITGA2B | c.3101A>G (p.Asp1034Gly) c.2415A>G c.294A>G c.78A>G c.2999A>G (p.Asp1000Gly) c.2984A>G (p.Asp995Gly) | gnomAD v4 |
17 | g.44372383T>G | CA399787709 | ITGA2B | c.3101A>C (p.Asp1034Ala) c.2415A>C c.294A>C c.78A>C c.2999A>C (p.Asp1000Ala) c.2984A>C (p.Asp995Ala) | |
17 | g.44372388_44372390del | CA290942822 | ITGA2B | c.3099_3101del (p.Glu1033del) c.2413_2415del c.292_294del c.76_78del c.2997_2999del (p.Glu999del) c.2982_2984del (p.Glu994del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372384C>A | CA399787715 | ITGA2B | c.3100G>T (p.Asp1034Tyr) c.2414G>T c.293G>T c.77G>T c.2998G>T (p.Asp1000Tyr) c.2983G>T (p.Asp995Tyr) | |
17 | g.44372384C= | CA2261364356 | ITGA2B | c.3100G= (p.Asp1034=) c.2414G= c.293G= c.77G= c.2998G= (p.Asp1000=) c.2983G= (p.Asp995=) | |
17 | g.44372384C>G | CA399787712 | ITGA2B | c.3100G>C (p.Asp1034His) c.2414G>C c.293G>C c.77G>C c.2998G>C (p.Asp1000His) c.2983G>C (p.Asp995His) | gnomAD v4 |
17 | g.44372384C>T | CA399787711 | ITGA2B | c.3100G>A (p.Asp1034Asn) c.2414G>A c.293G>A c.77G>A c.2998G>A (p.Asp1000Asn) c.2983G>A (p.Asp995Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372385T>A | CA290942825 | ITGA2B | c.3099A>T (p.Glu1033Asp) c.2413A>T c.292A>T c.76A>T c.2997A>T (p.Glu999Asp) c.2982A>T (p.Glu994Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372385T>C | CA500260629 | ITGA2B | c.3099A>G (p.Glu1033=) c.2413A>G c.292A>G c.76A>G c.2997A>G (p.Glu999=) c.2982A>G (p.Glu994=) | |
17 | g.44372385T>G | CA399787720 | ITGA2B | c.3099A>C (p.Glu1033Asp) c.2413A>C c.292A>C c.76A>C c.2997A>C (p.Glu999Asp) c.2982A>C (p.Glu994Asp) | |
17 | g.44372385T= | CA2261364357 | ITGA2B | c.3099A= (p.Glu1033=) c.2413A= c.292A= c.76A= c.2997A= (p.Glu999=) c.2982A= (p.Glu994=) | |
17 | g.44372386T>A | CA399787723 | ITGA2B | c.3098A>T (p.Glu1033Val) c.2412A>T c.291A>T c.75A>T c.2996A>T (p.Glu999Val) c.2981A>T (p.Glu994Val) | |
17 | g.44372386T>C | CA399787725 | ITGA2B | c.3098A>G (p.Glu1033Gly) c.2412A>G c.291A>G c.75A>G c.2996A>G (p.Glu999Gly) c.2981A>G (p.Glu994Gly) | |
17 | g.44372386T>G | CA399787728 | ITGA2B | c.3098A>C (p.Glu1033Ala) c.2412A>C c.291A>C c.75A>C c.2996A>C (p.Glu999Ala) c.2981A>C (p.Glu994Ala) | |
17 | g.44372387C>A | CA399787734 | ITGA2B | c.3097G>T (p.Glu1033Ter) c.2411G>T c.290G>T c.74G>T c.2995G>T (p.Glu999Ter) c.2980G>T (p.Glu994Ter) | |
17 | g.44372387C>G | CA399787736 | ITGA2B | c.3097G>C (p.Glu1033Gln) c.2411G>C c.290G>C c.74G>C c.2995G>C (p.Glu999Gln) c.2980G>C (p.Glu994Gln) | |
17 | g.44372387C>T | CA399787739 | ITGA2B | c.3097G>A (p.Glu1033Lys) c.2411G>A c.290G>A c.74G>A c.2995G>A (p.Glu999Lys) c.2980G>A (p.Glu994Lys) | |
17 | g.44372388T>A | CA399787743 | ITGA2B | c.3096A>T (p.Glu1032Asp) c.2410A>T c.289A>T c.73A>T c.2994A>T (p.Glu998Asp) c.2979A>T (p.Glu993Asp) | |
17 | g.44372388T>C | CA290942834 | ITGA2B | c.3096A>G (p.Glu1032=) c.2410A>G c.289A>G c.73A>G c.2994A>G (p.Glu998=) c.2979A>G (p.Glu993=) | dbSNP |
17 | g.44372388T>G | CA399787745 | ITGA2B | c.3096A>C (p.Glu1032Asp) c.2410A>C c.289A>C c.73A>C c.2994A>C (p.Glu998Asp) c.2979A>C (p.Glu993Asp) | |
17 | g.44372388T= | CA2261364358 | ITGA2B | c.3096A= (p.Glu1032=) c.2410A= c.289A= c.73A= c.2994A= (p.Glu998=) c.2979A= (p.Glu993=) | |
17 | g.44372389T>A | CA399787758 | ITGA2B | c.3095A>T (p.Glu1032Val) c.2409A>T c.288A>T c.72A>T c.2993A>T (p.Glu998Val) c.2978A>T (p.Glu993Val) | |
17 | g.44372389T>C | CA399787763 | ITGA2B | c.3095A>G (p.Glu1032Gly) c.2409A>G c.288A>G c.72A>G c.2993A>G (p.Glu998Gly) c.2978A>G (p.Glu993Gly) | |
17 | g.44372389T>G | CA399787766 | ITGA2B | c.3095A>C (p.Glu1032Ala) c.2409A>C c.288A>C c.72A>C c.2993A>C (p.Glu998Ala) c.2978A>C (p.Glu993Ala) | |
17 | g.44372390C>A | CA399787776 | ITGA2B | c.3094G>T (p.Glu1032Ter) c.2408G>T c.287G>T c.71G>T c.2992G>T (p.Glu998Ter) c.2977G>T (p.Glu993Ter) | |
17 | g.44372390C= | CA2261364359 | ITGA2B | c.3094G= (p.Glu1032=) c.2408G= c.287G= c.71G= c.2992G= (p.Glu998=) c.2977G= (p.Glu993=) | |
17 | g.44372390C>G | CA399787777 | ITGA2B | c.3094G>C (p.Glu1032Gln) c.2408G>C c.287G>C c.71G>C c.2992G>C (p.Glu998Gln) c.2977G>C (p.Glu993Gln) | |
17 | g.44372390C>T | CA399787770 | ITGA2B | c.3094G>A (p.Glu1032Lys) c.2408G>A c.287G>A c.71G>A c.2992G>A (p.Glu998Lys) c.2977G>A (p.Glu993Lys) | gnomAD v4 |
17 | g.44372391dup | CA915940756 | ITGA2B | c.3094dup (p.Glu1032GlyfsTer4) c.2408dup c.287dup c.71dup c.2992dup (p.Glu998GlyfsTer4) c.2977dup (p.Glu993GlyfsTer4) | |
17 | g.44372391C>A | CA500260675 | ITGA2B | c.3093G>T (p.Leu1031=) c.2407G>T c.286G>T c.70G>T c.2991G>T (p.Leu997=) c.2976G>T (p.Leu992=) | gnomAD v3 gnomAD v4 |
17 | g.44372391C>G | CA500260671 | ITGA2B | c.3093G>C (p.Leu1031=) c.2407G>C c.286G>C c.70G>C c.2991G>C (p.Leu997=) c.2976G>C (p.Leu992=) | |
17 | g.44372391C>T | CA500260674 | ITGA2B | c.3093G>A (p.Leu1031=) c.2407G>A c.286G>A c.70G>A c.2991G>A (p.Leu997=) c.2976G>A (p.Leu992=) | |
17 | g.44372391_44372392dup | CA500260678 | ITGA2B | c.3092_3093dup (p.Glu1032TrpfsTer?) c.2406_2407dup c.285_286dup c.69_70dup c.2990_2991dup (p.Glu998TrpfsTer?) c.2975_2976dup (p.Glu993TrpfsTer?) | ClinVar dbSNP gnomAD v4 |
17 | g.44372391_44372392insCA | CA2837995121 | ITGA2B | c.3092_3093insTG (p.Glu1032GlyfsTer?) c.2406_2407insTG c.285_286insTG c.69_70insTG c.2990_2991insTG (p.Glu998GlyfsTer?) c.2975_2976insTG (p.Glu993GlyfsTer?) | |
17 | g.44372392del | CA915940323 | ITGA2B | c.3092del (p.Leu1031ArgfsTer?) c.2406del c.285del c.69del c.2990del (p.Leu997ArgfsTer?) c.2975del (p.Leu992ArgfsTer?) | ClinVar dbSNP gnomAD v4 |
17 | g.44372392A= | CA2261364360 | ITGA2B | c.3092T= (p.Leu1031=) c.2406T= c.285T= c.69T= c.2990T= (p.Leu997=) c.2975T= (p.Leu992=) | |
17 | g.44372392A>C | CA399787779 | ITGA2B | c.3092T>G (p.Leu1031Arg) c.2406T>G c.285T>G c.69T>G c.2990T>G (p.Leu997Arg) c.2975T>G (p.Leu992Arg) | |
17 | g.44372392A>G | CA8602455 | ITGA2B | c.3092T>C (p.Leu1031Pro) c.2406T>C c.285T>C c.69T>C c.2990T>C (p.Leu997Pro) c.2975T>C (p.Leu992Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372392A>T | CA399787782 | ITGA2B | c.3092T>A (p.Leu1031Gln) c.2406T>A c.285T>A c.69T>A c.2990T>A (p.Leu997Gln) c.2975T>A (p.Leu992Gln) | |
17 | g.44372393G>A | CA500260685 | ITGA2B | c.3091C>T (p.Leu1031=) c.2405C>T c.284C>T c.68C>T c.2989C>T (p.Leu997=) c.2974C>T (p.Leu992=) | gnomAD v3 gnomAD v4 |
17 | g.44372393G>C | CA399787790 | ITGA2B | c.3091C>G (p.Leu1031Val) c.2405C>G c.284C>G c.68C>G c.2989C>G (p.Leu997Val) c.2974C>G (p.Leu992Val) | |
17 | g.44372393G>T | CA399787793 | ITGA2B | c.3091C>A (p.Leu1031Met) c.2405C>A c.284C>A c.68C>A c.2989C>A (p.Leu997Met) c.2974C>A (p.Leu992Met) | |
17 | g.44372396del | CA915940322 | ITGA2B | c.3091del (p.Leu1031TrpfsTer?) c.2405del c.284del c.68del c.2989del (p.Leu997TrpfsTer?) c.2974del (p.Leu992TrpfsTer?) | ClinVar |
17 | g.44372394G>A | CA500260695 | ITGA2B | c.3090C>T (p.Pro1030=) c.2404C>T c.283C>T c.67C>T c.2988C>T (p.Pro996=) c.2973C>T (p.Pro991=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372394G>C | CA500260696 | ITGA2B | c.3090C>G (p.Pro1030=) c.2404C>G c.283C>G c.67C>G c.2988C>G (p.Pro996=) c.2973C>G (p.Pro991=) | ClinVar dbSNP |
17 | g.44372394G= | CA2261364361 | ITGA2B | c.3090C= (p.Pro1030=) c.2404C= c.283C= c.67C= c.2988C= (p.Pro996=) c.2973C= (p.Pro991=) | |
17 | g.44372394G>T | CA500260697 | ITGA2B | c.3090C>A (p.Pro1030=) c.2404C>A c.283C>A c.67C>A c.2988C>A (p.Pro996=) c.2973C>A (p.Pro991=) | |
17 | g.44372395G>A | CA399787795 | ITGA2B | c.3089C>T (p.Pro1030Leu) c.2403C>T c.282C>T c.66C>T c.2987C>T (p.Pro996Leu) c.2972C>T (p.Pro991Leu) | gnomAD v4 |
17 | g.44372395G>C | CA399787798 | ITGA2B | c.3089C>G (p.Pro1030Arg) c.2403C>G c.282C>G c.66C>G c.2987C>G (p.Pro996Arg) c.2972C>G (p.Pro991Arg) | |
17 | g.44372395G>T | CA399787800 | ITGA2B | c.3089C>A (p.Pro1030His) c.2403C>A c.282C>A c.66C>A c.2987C>A (p.Pro996His) c.2972C>A (p.Pro991His) | |
17 | g.44372396G>A | CA8602456 | ITGA2B | c.3088C>T (p.Pro1030Ser) c.2402C>T c.281C>T c.65C>T c.2986C>T (p.Pro996Ser) c.2971C>T (p.Pro991Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44372396G>C | CA399787806 | ITGA2B | c.3088C>G (p.Pro1030Ala) c.2402C>G c.281C>G c.65C>G c.2986C>G (p.Pro996Ala) c.2971C>G (p.Pro991Ala) | gnomAD v4 |
17 | g.44372396G= | CA2261364362 | ITGA2B | c.3088C= (p.Pro1030=) c.2402C= c.281C= c.65C= c.2986C= (p.Pro996=) c.2971C= (p.Pro991=) | |
17 | g.44372396G>T | CA399787808 | ITGA2B | c.3088C>A (p.Pro1030Thr) c.2402C>A c.281C>A c.65C>A c.2986C>A (p.Pro996Thr) c.2971C>A (p.Pro991Thr) | gnomAD v4 |
17 | g.44372397T>A | CA500260706 | ITGA2B | c.3087A>T (p.Pro1029=) c.2401A>T c.280A>T c.64A>T c.2985A>T (p.Pro995=) c.2970A>T (p.Pro990=) | |
17 | g.44372397T>C | CA500260709 | ITGA2B | c.3087A>G (p.Pro1029=) c.2401A>G c.280A>G c.64A>G c.2985A>G (p.Pro995=) c.2970A>G (p.Pro990=) | |
17 | g.44372397T>G | CA500260710 | ITGA2B | c.3087A>C (p.Pro1029=) c.2401A>C c.280A>C c.64A>C c.2985A>C (p.Pro995=) c.2970A>C (p.Pro990=) | |
17 | g.44372398G>A | CA399787818 | ITGA2B | c.3086C>T (p.Pro1029Leu) c.2400C>T c.279C>T c.63C>T c.2984C>T (p.Pro995Leu) c.2969C>T (p.Pro990Leu) | |
17 | g.44372398G>C | CA399787815 | ITGA2B | c.3086C>G (p.Pro1029Arg) c.2400C>G c.279C>G c.63C>G c.2984C>G (p.Pro995Arg) c.2969C>G (p.Pro990Arg) | gnomAD v4 |
17 | g.44372398G>T | CA399787813 | ITGA2B | c.3086C>A (p.Pro1029Gln) c.2400C>A c.279C>A c.63C>A c.2984C>A (p.Pro995Gln) c.2969C>A (p.Pro990Gln) | |
17 | g.44372399G>A | CA399787821 | ITGA2B | c.3085C>T (p.Pro1029Ser) c.2399C>T c.278C>T c.62C>T c.2983C>T (p.Pro995Ser) c.2968C>T (p.Pro990Ser) | |
17 | g.44372399G>C | CA399787824 | ITGA2B | c.3085C>G (p.Pro1029Ala) c.2399C>G c.278C>G c.62C>G c.2983C>G (p.Pro995Ala) c.2968C>G (p.Pro990Ala) | |
17 | g.44372399G= | CA2261364363 | ITGA2B | c.3085C= (p.Pro1029=) c.2399C= c.278C= c.62C= c.2983C= (p.Pro995=) c.2968C= (p.Pro990=) | |
17 | g.44372399G>T | CA399787827 | ITGA2B | c.3085C>A (p.Pro1029Thr) c.2399C>A c.278C>A c.62C>A c.2983C>A (p.Pro995Thr) c.2968C>A (p.Pro990Thr) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44372400C>A | CA500260721 | ITGA2B | c.3084G>T (p.Arg1028=) c.2398G>T c.277G>T c.61G>T c.2982G>T (p.Arg994=) c.2967G>T (p.Arg989=) | |
17 | g.44372400C>G | CA500260722 | ITGA2B | c.3084G>C (p.Arg1028=) c.2398G>C c.277G>C c.61G>C c.2982G>C (p.Arg994=) c.2967G>C (p.Arg989=) | |
17 | g.44372400C>T | CA500260724 | ITGA2B | c.3084G>A (p.Arg1028=) c.2398G>A c.277G>A c.61G>A c.2982G>A (p.Arg994=) c.2967G>A (p.Arg989=) | COSMIC |
17 | g.44372401C>A | CA399787831 | ITGA2B | c.3083G>T (p.Arg1028Leu) c.2397G>T c.276G>T c.60G>T c.2981G>T (p.Arg994Leu) c.2966G>T (p.Arg989Leu) | |
17 | g.44372401C= | CA2261364364 | ITGA2B | c.3083G= (p.Arg1028=) c.2397G= c.276G= c.60G= c.2981G= (p.Arg994=) c.2966G= (p.Arg989=) | |
17 | g.44372401C>G | CA399787834 | ITGA2B | c.3083G>C (p.Arg1028Pro) c.2397G>C c.276G>C c.60G>C c.2981G>C (p.Arg994Pro) c.2966G>C (p.Arg989Pro) | |
17 | g.44372401C>T | CA8602457 | ITGA2B | c.3083G>A (p.Arg1028Gln) c.2397G>A c.276G>A c.60G>A c.2981G>A (p.Arg994Gln) c.2966G>A (p.Arg989Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372402G>A | CA8602458 | ITGA2B | c.3082C>T (p.Arg1028Trp) c.2396C>T c.275C>T c.59C>T c.2980C>T (p.Arg994Trp) c.2965C>T (p.Arg989Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44372402G>C | CA399787837 | ITGA2B | c.3082C>G (p.Arg1028Gly) c.2396C>G c.275C>G c.59C>G c.2980C>G (p.Arg994Gly) c.2965C>G (p.Arg989Gly) | |
17 | g.44372402G= | CA2261364365 | ITGA2B | c.3082C= (p.Arg1028=) c.2396C= c.275C= c.59C= c.2980C= (p.Arg994=) c.2965C= (p.Arg989=) | |
17 | g.44372402G>T | CA500260727 | ITGA2B | c.3082C>A (p.Arg1028=) c.2396C>A c.275C>A c.59C>A c.2980C>A (p.Arg994=) c.2965C>A (p.Arg989=) | |
17 | g.44372403G>A | CA500260732 | ITGA2B | c.3081C>T (p.Asn1027=) c.2395C>T c.274C>T c.58C>T c.2979C>T (p.Asn993=) c.2964C>T (p.Asn988=) | |
17 | g.44372403G>C | CA399787839 | ITGA2B | c.3081C>G (p.Asn1027Lys) c.2395C>G c.274C>G c.58C>G c.2979C>G (p.Asn993Lys) c.2964C>G (p.Asn988Lys) | |
17 | g.44372403G>T | CA399787840 | ITGA2B | c.3081C>A (p.Asn1027Lys) c.2395C>A c.274C>A c.58C>A c.2979C>A (p.Asn993Lys) c.2964C>A (p.Asn988Lys) | |
17 | g.44372404T>A | CA399787842 | ITGA2B | c.3080A>T (p.Asn1027Ile) c.2394A>T c.273A>T c.57A>T c.2978A>T (p.Asn993Ile) c.2963A>T (p.Asn988Ile) | |
17 | g.44372404T>C | CA399787843 | ITGA2B | c.3080A>G (p.Asn1027Ser) c.2394A>G c.273A>G c.57A>G c.2978A>G (p.Asn993Ser) c.2963A>G (p.Asn988Ser) | |
17 | g.44372404T>G | CA399787844 | ITGA2B | c.3080A>C (p.Asn1027Thr) c.2394A>C c.273A>C c.57A>C c.2978A>C (p.Asn993Thr) c.2963A>C (p.Asn988Thr) | |
17 | g.44372405T>A | CA399787849 | ITGA2B | c.3079A>T (p.Asn1027Tyr) c.2393A>T c.272A>T c.56A>T c.2977A>T (p.Asn993Tyr) c.2962A>T (p.Asn988Tyr) | |
17 | g.44372405T>C | CA399787852 | ITGA2B | c.3079A>G (p.Asn1027Asp) c.2393A>G c.272A>G c.56A>G c.2977A>G (p.Asn993Asp) c.2962A>G (p.Asn988Asp) | |
17 | g.44372405T>G | CA399787847 | ITGA2B | c.3079A>C (p.Asn1027His) c.2393A>C c.272A>C c.56A>C c.2977A>C (p.Asn993His) c.2962A>C (p.Asn988His) | |
17 | g.44372406C>A | CA500260746 | ITGA2B | c.3078G>T (p.Arg1026=) c.2392G>T c.271G>T c.55G>T c.2976G>T (p.Arg992=) c.2961G>T (p.Arg987=) | |
17 | g.44372406C>G | CA500260749 | ITGA2B | c.3078G>C (p.Arg1026=) c.2392G>C c.271G>C c.55G>C c.2976G>C (p.Arg992=) c.2961G>C (p.Arg987=) | |
17 | g.44372406C>T | CA500260752 | ITGA2B | c.3078G>A (p.Arg1026=) c.2392G>A c.271G>A c.55G>A c.2976G>A (p.Arg992=) c.2961G>A (p.Arg987=) | COSMIC |
17 | g.44372407C>A | CA399787855 | ITGA2B | c.3077G>T (p.Arg1026Leu) c.2391G>T c.270G>T c.54G>T c.2975G>T (p.Arg992Leu) c.2960G>T (p.Arg987Leu) | ClinVar |
17 | g.44372407C= | CA2261364366 | ITGA2B | c.3077G= (p.Arg1026=) c.2391G= c.270G= c.54G= c.2975G= (p.Arg992=) c.2960G= (p.Arg987=) | |
17 | g.44372407C>G | CA399787853 | ITGA2B | c.3077G>C (p.Arg1026Pro) c.2391G>C c.270G>C c.54G>C c.2975G>C (p.Arg992Pro) c.2960G>C (p.Arg987Pro) | |
17 | g.44372407C>T | CA10575572 | ITGA2B | c.3077G>A (p.Arg1026Gln) c.2391G>A c.270G>A c.54G>A c.2975G>A (p.Arg992Gln) c.2960G>A (p.Arg987Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.44372407_44372408delinsCG | CA2261364367 | ITGA2B | c.3076_3077delinsCG (p.Arg1026=) c.2390_2391delinsCG c.269_270delinsCG c.53_54delinsCG c.2974_2975delinsCG (p.Arg992=) c.2959_2960delinsCG (p.Arg987=) | |
17 | g.44372407_44372408delinsGC | CA915940802 | ITGA2B | c.3076_3077delinsGC (p.Arg1026Ala) c.2390_2391delinsGC c.269_270delinsGC c.53_54delinsGC c.2974_2975delinsGC (p.Arg992Ala) c.2959_2960delinsGC (p.Arg987Ala) | ClinVar dbSNP |
17 | g.44372408G>A | CA10575573 | ITGA2B | c.3076C>T (p.Arg1026Trp) c.2390C>T c.269C>T c.53C>T c.2974C>T (p.Arg992Trp) c.2959C>T (p.Arg987Trp) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.44372408G>C | CA399787861 | ITGA2B | c.3076C>G (p.Arg1026Gly) c.2390C>G c.269C>G c.53C>G c.2974C>G (p.Arg992Gly) c.2959C>G (p.Arg987Gly) | |
17 | g.44372408G= | CA2261364368 | ITGA2B | c.3076C= (p.Arg1026=) c.2390C= c.269C= c.53C= c.2974C= (p.Arg992=) c.2959C= (p.Arg987=) | |
17 | g.44372408G>T | CA8602459 | ITGA2B | c.3076C>A (p.Arg1026=) c.2390C>A c.269C>A c.53C>A c.2974C>A (p.Arg992=) c.2959C>A (p.Arg987=) | dbSNP ExAC gnomAD v2 gnomAD v4 |