| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.44379787T>A | CA399801910 | ITGA2B | c.1780A>T (p.Ser594Cys) c.1211A>T n.575A>T | |
| 17 | g.44379787T>C | CA399801911 | ITGA2B | c.1780A>G (p.Ser594Gly) c.1211A>G n.575A>G | |
| 17 | g.44379787T>G | CA399801909 | ITGA2B | c.1780A>C (p.Ser594Arg) c.1211A>C n.575A>C | |
| 17 | g.44379788C>A | CA500272137 | ITGA2B | c.1779G>T (p.Leu593=) c.1210G>T n.574G>T | |
| 17 | g.44379788C= | CA2261367803 | ITGA2B | c.1779G= (p.Leu593=) c.1210G= n.574G= | |
| 17 | g.44379788C>G | CA8602941 | ITGA2B | c.1779G>C (p.Leu593=) c.1210G>C n.574G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.44379788C>T | CA500272139 | ITGA2B | c.1779G>A (p.Leu593=) c.1210G>A n.574G>A | |
| 17 | g.44379789A>C | CA399801912 | ITGA2B | c.1778T>G (p.Leu593Arg) c.1209T>G n.573T>G | |
| 17 | g.44379789A>G | CA399801913 | ITGA2B | c.1778T>C (p.Leu593Pro) c.1209T>C n.573T>C | |
| 17 | g.44379789A>T | CA399801914 | ITGA2B | c.1778T>A (p.Leu593Gln) c.1209T>A n.573T>A | |
| 17 | g.44379790G>A | CA500272147 | ITGA2B | c.1777C>T (p.Leu593=) c.1208C>T n.572C>T | gnomAD v4 |
| 17 | g.44379790G>C | CA290949643 | ITGA2B | c.1777C>G (p.Leu593Val) c.1208C>G n.572C>G | dbSNP gnomAD v2 |
| 17 | g.44379790G= | CA2261367804 | ITGA2B | c.1777C= (p.Leu593=) c.1208C= n.572C= | |
| 17 | g.44379790G>T | CA399801915 | ITGA2B | c.1777C>A (p.Leu593Met) c.1208C>A n.572C>A | |
| 17 | g.44379791C>A | CA290949646 | ITGA2B | c.1776G>T (p.Lys592Asn) c.1207G>T n.571G>T | dbSNP |
| 17 | g.44379791C= | CA2261367805 | ITGA2B | c.1776G= (p.Lys592=) c.1207G= n.571G= | |
| 17 | g.44379791C>G | CA399801916 | ITGA2B | c.1776G>C (p.Lys592Asn) c.1207G>C n.571G>C | |
| 17 | g.44379791C>T | CA500272167 | ITGA2B | c.1776G>A (p.Lys592=) c.1207G>A n.571G>A | |
| 17 | g.44379792T>A | CA399801917 | ITGA2B | c.1775A>T (p.Lys592Met) c.1206A>T n.570A>T | |
| 17 | g.44379792T>C | CA399801918 | ITGA2B | c.1775A>G (p.Lys592Arg) c.1206A>G n.570A>G | |
| 17 | g.44379792T>G | CA399801919 | ITGA2B | c.1775A>C (p.Lys592Thr) c.1206A>C n.570A>C | |
| 17 | g.44379793T>A | CA399801920 | ITGA2B | c.1774A>T (p.Lys592Ter) c.1205A>T n.569A>T | |
| 17 | g.44379793T>C | CA399801921 | ITGA2B | c.1774A>G (p.Lys592Glu) c.1205A>G n.569A>G | gnomAD v4 |
| 17 | g.44379793T>G | CA399801922 | ITGA2B | c.1774A>C (p.Lys592Gln) c.1205A>C n.569A>C | |
| 17 | g.44379794G>A | CA500272195 | ITGA2B | c.1773C>T (p.Asp591=) c.1204C>T n.568C>T | |
| 17 | g.44379794G>C | CA399801924 | ITGA2B | c.1773C>G (p.Asp591Glu) c.1204C>G n.568C>G | dbSNP gnomAD v4 |
| 17 | g.44379794G= | CA2261367806 | ITGA2B | c.1773C= (p.Asp591=) c.1204C= n.568C= | |
| 17 | g.44379794G>T | CA399801923 | ITGA2B | c.1773C>A (p.Asp591Glu) c.1204C>A n.568C>A | |
| 17 | g.44379795T>A | CA399801925 | ITGA2B | c.1772A>T (p.Asp591Val) c.1203A>T n.567A>T | |
| 17 | g.44379795T>C | CA399801926 | ITGA2B | c.1772A>G (p.Asp591Gly) c.1203A>G n.567A>G | |
| 17 | g.44379795T>G | CA8602942 | ITGA2B | c.1772A>C (p.Asp591Ala) c.1203A>C n.567A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.44379795T= | CA2261367807 | ITGA2B | c.1772A= (p.Asp591=) c.1203A= n.567A= | |
| 17 | g.44379796C>A | CA399801927 | ITGA2B | c.1771G>T (p.Asp591Tyr) c.1202G>T n.566G>T | |
| 17 | g.44379796C>G | CA399801928 | ITGA2B | c.1771G>C (p.Asp591His) c.1202G>C n.566G>C | gnomAD v4 |
| 17 | g.44379796C>T | CA399801929 | ITGA2B | c.1771G>A (p.Asp591Asn) c.1202G>A n.566G>A | gnomAD v4 |
| 17 | g.44379798dup | CA915940334 | ITGA2B | c.1771dup (p.Asp591GlyfsTer?) c.1202dup n.566dup | ClinVar |
| 17 | g.44379797C>A | CA500272214 | ITGA2B | c.1770G>T (p.Arg590=) c.1201G>T n.565G>T | |
| 17 | g.44379797C= | CA2261367808 | ITGA2B | c.1770G= (p.Arg590=) c.1201G= n.565G= | |
| 17 | g.44379797C>G | CA500272218 | ITGA2B | c.1770G>C (p.Arg590=) c.1201G>C n.565G>C | |
| 17 | g.44379797C>T | CA500272219 | ITGA2B | c.1770G>A (p.Arg590=) c.1201G>A n.565G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.44379798C>A | CA399801930 | ITGA2B | c.1769G>T (p.Arg590Leu) c.1200G>T n.564G>T | |
| 17 | g.44379798C= | CA2261367809 | ITGA2B | c.1769G= (p.Arg590=) c.1200G= n.564G= | |
| 17 | g.44379798C>G | CA399801931 | ITGA2B | c.1769G>C (p.Arg590Pro) c.1200G>C n.564G>C | |
| 17 | g.44379798C>T | CA8602943 | ITGA2B | c.1769G>A (p.Arg590Gln) c.1200G>A n.564G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.44379799G>A | CA8602944 | ITGA2B | c.1768C>T (p.Arg590Trp) c.1199C>T n.563C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.44379799G>C | CA399801932 | ITGA2B | c.1768C>G (p.Arg590Gly) c.1199C>G n.563C>G | |
| 17 | g.44379799G= | CA2261367810 | ITGA2B | c.1768C= (p.Arg590=) c.1199C= n.563C= | |
| 17 | g.44379799G>T | CA500272231 | ITGA2B | c.1768C>A (p.Arg590=) c.1199C>A n.563C>A | |
| 17 | g.44379800G>A | CA500272238 | ITGA2B | c.1767C>T (p.Phe589=) c.1198C>T n.562C>T | COSMIC |
| 17 | g.44379800G>C | CA399801933 | ITGA2B | c.1767C>G (p.Phe589Leu) c.1198C>G n.562C>G |