Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130862763_130863035del | CA645556968 | ABL1 | c.607_879del c.550_822del | COSMIC |
9 | g.130862790A= | CA1881463013 | ABL1 | c.634A= (p.Asn212=) c.577A= (p.Asn193=) | |
9 | g.130862790A>C | CA5285251 | ABL1 | c.634A>C (p.Asn212His) c.577A>C (p.Asn193His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.130862790A>G | CA375262366 | ABL1 | c.634A>G (p.Asn212Asp) c.577A>G (p.Asn193Asp) | |
9 | g.130862790A>T | CA375262367 | ABL1 | c.634A>T (p.Asn212Tyr) c.577A>T (p.Asn193Tyr) | |
9 | g.130862791A= | CA1881463016 | ABL1 | c.635A= (p.Asn212=) c.578A= (p.Asn193=) | |
9 | g.130862791A>C | CA375262370 | ABL1 | c.635A>C (p.Asn212Thr) c.578A>C (p.Asn193Thr) | |
9 | g.130862791A>G | CA5285252 | ABL1 | c.635A>G (p.Asn212Ser) c.578A>G (p.Asn193Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.130862791A>T | CA375262373 | ABL1 | c.635A>T (p.Asn212Ile) c.578A>T (p.Asn193Ile) | |
9 | g.130862792C>A | CA375262375 | ABL1 | c.636C>A (p.Asn212Lys) c.579C>A (p.Asn193Lys) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.130862792C= | CA1881463019 | ABL1 | c.636C= (p.Asn212=) c.579C= (p.Asn193=) | |
9 | g.130862792C>G | CA375262376 | ABL1 | c.636C>G (p.Asn212Lys) c.579C>G (p.Asn193Lys) | |
9 | g.130862792C>T | CA467496191 | ABL1 | c.636C>T (p.Asn212=) c.579C>T (p.Asn193=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.130862793A= | CA1881463022 | ABL1 | c.637A= (p.Thr213=) c.580A= (p.Thr194=) | |
9 | g.130862793A>C | CA375262377 | ABL1 | c.637A>C (p.Thr213Pro) c.580A>C (p.Thr194Pro) | dbSNP |
9 | g.130862793A>G | CA375262378 | ABL1 | c.637A>G (p.Thr213Ala) c.580A>G (p.Thr194Ala) | dbSNP gnomAD v4 |
9 | g.130862793A>T | CA375262379 | ABL1 | c.637A>T (p.Thr213Ser) c.580A>T (p.Thr194Ser) | dbSNP |
9 | g.130862794C>A | CA375262384 | ABL1 | c.638C>A (p.Thr213Asn) c.581C>A (p.Thr194Asn) | gnomAD v4 |
9 | g.130862794C>G | CA375262382 | ABL1 | c.638C>G (p.Thr213Ser) c.581C>G (p.Thr194Ser) | |
9 | g.130862794C>T | CA375262380 | ABL1 | c.638C>T (p.Thr213Ile) c.581C>T (p.Thr194Ile) | gnomAD v4 |
9 | g.130862794_130862795insAGGACAGAGTGTTTAGAAGATCACTT | CA2720751427 | ABL1 | c.638_639insAGGACAGAGTGTTTAGAAGATCACTT (p.Leu214GlyfsTer5) c.581_582insAGGACAGAGTGTTTAGAAGATCACTT (p.Leu195GlyfsTer5) | dbSNP |
9 | g.130862795C>A | CA467496195 | ABL1 | c.639C>A (p.Thr213=) c.582C>A (p.Thr194=) | |
9 | g.130862795C= | CA1881463031 | ABL1 | c.639C= (p.Thr213=) c.582C= (p.Thr194=) | |
9 | g.130862795C>G | CA467496197 | ABL1 | c.639C>G (p.Thr213=) c.582C>G (p.Thr194=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.130862795C>T | CA467496199 | ABL1 | c.639C>T (p.Thr213=) c.582C>T (p.Thr194=) | |
9 | g.130862796C>A | CA375262385 | ABL1 | c.640C>A (p.Leu214Met) c.583C>A (p.Leu195Met) | |
9 | g.130862796C= | CA1881463037 | ABL1 | c.640C= (p.Leu214=) c.583C= (p.Leu195=) | |
9 | g.130862796C>G | CA375262387 | ABL1 | c.640C>G (p.Leu214Val) c.583C>G (p.Leu195Val) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.130862796C>T | CA467496200 | ABL1 | c.640C>T (p.Leu214=) c.583C>T (p.Leu195=) | gnomAD v4 |
9 | g.130862797T>A | CA375262390 | ABL1 | c.641T>A (p.Leu214Gln) c.584T>A (p.Leu195Gln) | dbSNP |
9 | g.130862797T>C | CA375262393 | ABL1 | c.641T>C (p.Leu214Pro) c.584T>C (p.Leu195Pro) | |
9 | g.130862797T>G | CA375262391 | ABL1 | c.641T>G (p.Leu214Arg) c.584T>G (p.Leu195Arg) | |
9 | g.130862798G>A | CA467496205 | ABL1 | c.642G>A (p.Leu214=) c.585G>A (p.Leu195=) | dbSNP |
9 | g.130862798G>C | CA467496207 | ABL1 | c.642G>C (p.Leu214=) c.585G>C (p.Leu195=) | |
9 | g.130862798G= | CA1881463041 | ABL1 | c.642G= (p.Leu214=) c.585G= (p.Leu195=) | |
9 | g.130862798G>T | CA467496208 | ABL1 | c.642G>T (p.Leu214=) c.585G>T (p.Leu195=) | |
9 | g.130862799G>A | CA375262395 | ABL1 | c.643G>A (p.Ala215Thr) c.586G>A (p.Ala196Thr) | dbSNP |
9 | g.130862799G>C | CA5285253 | ABL1 | c.643G>C (p.Ala215Pro) c.586G>C (p.Ala196Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.130862799G= | CA1881463044 | ABL1 | c.643G= (p.Ala215=) c.586G= (p.Ala196=) | |
9 | g.130862799G>T | CA375262398 | ABL1 | c.643G>T (p.Ala215Ser) c.586G>T (p.Ala196Ser) | |
9 | g.130862800C>A | CA375262400 | ABL1 | c.644C>A (p.Ala215Asp) c.587C>A (p.Ala196Asp) | |
9 | g.130862800C>G | CA375262402 | ABL1 | c.644C>G (p.Ala215Gly) c.587C>G (p.Ala196Gly) | |
9 | g.130862800C>T | CA375262404 | ABL1 | c.644C>T (p.Ala215Val) c.587C>T (p.Ala196Val) | |
9 | g.130862801C>A | CA467496216 | ABL1 | c.645C>A (p.Ala215=) c.588C>A (p.Ala196=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.130862801C= | CA1881463049 | ABL1 | c.645C= (p.Ala215=) c.588C= (p.Ala196=) | |
9 | g.130862801C>G | CA5285255 | ABL1 | c.645C>G (p.Ala215=) c.588C>G (p.Ala196=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.130862801C>T | CA5285254 | ABL1 | c.645C>T (p.Ala215=) c.588C>T (p.Ala196=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.130862802G>A | CA5285256 | ABL1 | c.646G>A (p.Glu216Lys) c.589G>A (p.Glu197Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.130862802G>C | CA375262409 | ABL1 | c.646G>C (p.Glu216Gln) c.589G>C (p.Glu197Gln) | dbSNP gnomAD v4 |
9 | g.130862802G= | CA1881463058 | ABL1 | c.646G= (p.Glu216=) c.589G= (p.Glu197=) |