Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.44379791C>ACA290949646ITGA2Bc.1776G>T (p.Lys592Asn)
c.1207G>T
n.571G>T
 dbSNP
17g.44379791C=CA2261367805ITGA2Bc.1776G= (p.Lys592=)
c.1207G=
n.571G=
17g.44379791C>GCA399801916ITGA2Bc.1776G>C (p.Lys592Asn)
c.1207G>C
n.571G>C
17g.44379791C>TCA500272167ITGA2Bc.1776G>A (p.Lys592=)
c.1207G>A
n.571G>A
17g.44379792T>ACA399801917ITGA2Bc.1775A>T (p.Lys592Met)
c.1206A>T
n.570A>T
17g.44379792T>CCA399801918ITGA2Bc.1775A>G (p.Lys592Arg)
c.1206A>G
n.570A>G
17g.44379792T>GCA399801919ITGA2Bc.1775A>C (p.Lys592Thr)
c.1206A>C
n.570A>C
17g.44379793T>ACA399801920ITGA2Bc.1774A>T (p.Lys592Ter)
c.1205A>T
n.569A>T
17g.44379793T>CCA399801921ITGA2Bc.1774A>G (p.Lys592Glu)
c.1205A>G
n.569A>G
 gnomAD v4
17g.44379793T>GCA399801922ITGA2Bc.1774A>C (p.Lys592Gln)
c.1205A>C
n.569A>C
17g.44379794G>ACA500272195ITGA2Bc.1773C>T (p.Asp591=)
c.1204C>T
n.568C>T
17g.44379794G>CCA399801924ITGA2Bc.1773C>G (p.Asp591Glu)
c.1204C>G
n.568C>G
 dbSNP gnomAD v4
17g.44379794G=CA2261367806ITGA2Bc.1773C= (p.Asp591=)
c.1204C=
n.568C=
17g.44379794G>TCA399801923ITGA2Bc.1773C>A (p.Asp591Glu)
c.1204C>A
n.568C>A
17g.44379795T>ACA399801925ITGA2Bc.1772A>T (p.Asp591Val)
c.1203A>T
n.567A>T
17g.44379795T>CCA399801926ITGA2Bc.1772A>G (p.Asp591Gly)
c.1203A>G
n.567A>G
17g.44379795T>GCA8602942ITGA2Bc.1772A>C (p.Asp591Ala)
c.1203A>C
n.567A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44379795T=CA2261367807ITGA2Bc.1772A= (p.Asp591=)
c.1203A=
n.567A=
17g.44379796C>ACA399801927ITGA2Bc.1771G>T (p.Asp591Tyr)
c.1202G>T
n.566G>T
17g.44379796C>GCA399801928ITGA2Bc.1771G>C (p.Asp591His)
c.1202G>C
n.566G>C
 gnomAD v4
17g.44379796C>TCA399801929ITGA2Bc.1771G>A (p.Asp591Asn)
c.1202G>A
n.566G>A
 gnomAD v4
17g.44379798dupCA915940334ITGA2Bc.1771dup (p.Asp591GlyfsTer?)
c.1202dup
n.566dup
 ClinVar
17g.44379797C>ACA500272214ITGA2Bc.1770G>T (p.Arg590=)
c.1201G>T
n.565G>T
17g.44379797C=CA2261367808ITGA2Bc.1770G= (p.Arg590=)
c.1201G=
n.565G=
17g.44379797C>GCA500272218ITGA2Bc.1770G>C (p.Arg590=)
c.1201G>C
n.565G>C
17g.44379797C>TCA500272219ITGA2Bc.1770G>A (p.Arg590=)
c.1201G>A
n.565G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.44379798C>ACA399801930ITGA2Bc.1769G>T (p.Arg590Leu)
c.1200G>T
n.564G>T
17g.44379798C=CA2261367809ITGA2Bc.1769G= (p.Arg590=)
c.1200G=
n.564G=
17g.44379798C>GCA399801931ITGA2Bc.1769G>C (p.Arg590Pro)
c.1200G>C
n.564G>C
17g.44379798C>TCA8602943ITGA2Bc.1769G>A (p.Arg590Gln)
c.1200G>A
n.564G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.44379799G>ACA8602944ITGA2Bc.1768C>T (p.Arg590Trp)
c.1199C>T
n.563C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.44379799G>CCA399801932ITGA2Bc.1768C>G (p.Arg590Gly)
c.1199C>G
n.563C>G
17g.44379799G=CA2261367810ITGA2Bc.1768C= (p.Arg590=)
c.1199C=
n.563C=
17g.44379799G>TCA500272231ITGA2Bc.1768C>A (p.Arg590=)
c.1199C>A
n.563C>A
17g.44379800G>ACA500272238ITGA2Bc.1767C>T (p.Phe589=)
c.1198C>T
n.562C>T
 COSMIC
17g.44379800G>CCA399801933ITGA2Bc.1767C>G (p.Phe589Leu)
c.1198C>G
n.562C>G
17g.44379800G>TCA399801935ITGA2Bc.1767C>A (p.Phe589Leu)
c.1198C>A
n.562C>A
17g.44379801A>CCA399801939ITGA2Bc.1766T>G (p.Phe589Cys)
c.1197T>G
n.561T>G
17g.44379801A>GCA399801938ITGA2Bc.1766T>C (p.Phe589Ser)
c.1197T>C
n.561T>C
17g.44379801A>TCA399801937ITGA2Bc.1766T>A (p.Phe589Tyr)
c.1197T>A
n.561T>A
17g.44379802A>CCA399801942ITGA2Bc.1765T>G (p.Phe589Val)
c.1196T>G
n.560T>G
17g.44379802A>GCA399801940ITGA2Bc.1765T>C (p.Phe589Leu)
c.1196T>C
n.560T>C
17g.44379802A>TCA399801941ITGA2Bc.1765T>A (p.Phe589Ile)
c.1196T>A
n.560T>A
17g.44379803G>ACA500272255ITGA2Bc.1764C>T (p.Asp588=)
c.1195C>T
n.559C>T
17g.44379803G>CCA399801944ITGA2Bc.1764C>G (p.Asp588Glu)
c.1195C>G
n.559C>G
17g.44379803G>TCA399801947ITGA2Bc.1764C>A (p.Asp588Glu)
c.1195C>A
n.559C>A
 gnomAD v4
17g.44379804T>ACA399801948ITGA2Bc.1763A>T (p.Asp588Val)
c.1194A>T
n.558A>T
17g.44379804T>CCA399801951ITGA2Bc.1763A>G (p.Asp588Gly)
c.1194A>G
n.558A>G
17g.44379804T>GCA399801953ITGA2Bc.1763A>C (p.Asp588Ala)
c.1194A>C
n.558A>C
17g.44379805C>ACA399801955ITGA2Bc.1762G>T (p.Asp588Tyr)
c.1193G>T
n.557G>T

Number of alleles fetched