Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7579597del | CA2573131738 | DSP | c.3407del (p.Lys1136ArgfsTer23) | |
6 | g.7579597A>C | CA362683976 | DSP | c.3407A>C (p.Lys1136Thr) | |
6 | g.7579597A>G | CA362683977 | DSP | c.3407A>G (p.Lys1136Arg) | |
6 | g.7579597A>T | CA362683978 | DSP | c.3407A>T (p.Lys1136Met) | |
6 | g.7579598G>A | CA448714079 | DSP | c.3408G>A (p.Lys1136=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7579598G>C | CA362683980 | DSP | c.3408G>C (p.Lys1136Asn) | |
6 | g.7579598G= | CA1608614258 | DSP | c.3408G= (p.Lys1136=) | |
6 | g.7579598G>T | CA362683979 | DSP | c.3408G>T (p.Lys1136Asn) | |
6 | g.7579598_7579599delinsAG | CA913187624 | DSP | c.3408_3409delinsAG (p.Asn1137Asp) | ClinVar dbSNP |
6 | g.7579598_7579599delinsGA | CA1608614261 | DSP | c.3408_3409delinsGA (p.Lys1136=) | |
6 | g.7579599A= | CA1608614266 | DSP | c.3409A= (p.Asn1137=) | |
6 | g.7579599A>C | CA362683981 | DSP | c.3409A>C (p.Asn1137His) | |
6 | g.7579599A>G | CA362683982 | DSP | c.3409A>G (p.Asn1137Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7579599A>T | CA362683983 | DSP | c.3409A>T (p.Asn1137Tyr) | |
6 | g.7579600A>C | CA362683984 | DSP | c.3410A>C (p.Asn1137Thr) | |
6 | g.7579600A>G | CA362683985 | DSP | c.3410A>G (p.Asn1137Ser) | |
6 | g.7579600A>T | CA362683986 | DSP | c.3410A>T (p.Asn1137Ile) | |
6 | g.7579601T>A | CA362683987 | DSP | c.3411T>A (p.Asn1137Lys) | |
6 | g.7579601T>C | CA448714084 | DSP | c.3411T>C (p.Asn1137=) | |
6 | g.7579601T>G | CA362683988 | DSP | c.3411T>G (p.Asn1137Lys) | |
6 | g.7579602G>A | CA362683989 | DSP | c.3412G>A (p.Asp1138Asn) | |
6 | g.7579602G>C | CA362683990 | DSP | c.3412G>C (p.Asp1138His) | |
6 | g.7579602G>T | CA362683991 | DSP | c.3412G>T (p.Asp1138Tyr) | |
6 | g.7579603A= | CA1608614271 | DSP | c.3413A= (p.Asp1138=) | |
6 | g.7579603A>C | CA362683992 | DSP | c.3413A>C (p.Asp1138Ala) | |
6 | g.7579603A>G | CA362683993 | DSP | c.3413A>G (p.Asp1138Gly) | dbSNP gnomAD v2 |
6 | g.7579603A>T | CA362683994 | DSP | c.3413A>T (p.Asp1138Val) | |
6 | g.7579604C>A | CA362683995 | DSP | c.3414C>A (p.Asp1138Glu) | |
6 | g.7579604C= | CA1608614281 | DSP | c.3414C= (p.Asp1138=) | |
6 | g.7579604C>G | CA362683996 | DSP | c.3414C>G (p.Asp1138Glu) | |
6 | g.7579604C>T | CA038078 | DSP | c.3414C>T (p.Asp1138=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7579604_7579607delinsCTAT | CA1608614282 | DSP | c.3414_3417delinsCTAT (p.Asp1138=) | |
6 | g.7579605T>A | CA362683997 | DSP | c.3415T>A (p.Tyr1139Asn) | |
6 | g.7579605T>C | CA362683999 | DSP | c.3415T>C (p.Tyr1139His) | |
6 | g.7579605T>G | CA362683998 | DSP | c.3415T>G (p.Tyr1139Asp) | COSMIC |
6 | g.7579605dup | CA2677226030 | DSP | c.3415dup (p.Tyr1139LeufsTer2) | gnomAD v4 |
6 | g.7579605_7579607delinsG | CA16618323 | DSP | c.3415_3417delinsG (p.Tyr1139GlyfsTer10) | ClinVar dbSNP |
6 | g.7579606A= | CA1608614291 | DSP | c.3416A= (p.Tyr1139=) | |
6 | g.7579606A>C | CA362684000 | DSP | c.3416A>C (p.Tyr1139Ser) | |
6 | g.7579606A>G | CA362684002 | DSP | c.3416A>G (p.Tyr1139Cys) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7579606A>T | CA362684001 | DSP | c.3416A>T (p.Tyr1139Phe) | |
6 | g.7579607T>A | CA362684003 | DSP | c.3417T>A (p.Tyr1139Ter) | |
6 | g.7579607T>C | CA448714088 | DSP | c.3417T>C (p.Tyr1139=) | |
6 | g.7579607T>G | CA362684004 | DSP | c.3417T>G (p.Tyr1139Ter) | |
6 | g.7579608G>A | CA362684005 | DSP | c.3418G>A (p.Asp1140Asn) | |
6 | g.7579608G>C | CA362684006 | DSP | c.3418G>C (p.Asp1140His) | |
6 | g.7579608G>T | CA362684007 | DSP | c.3418G>T (p.Asp1140Tyr) | gnomAD v4 |
6 | g.7579608_7579609delinsGA | CA1608614295 | DSP | c.3418_3419delinsGA (p.Asp1140=) | |
6 | g.7579609del | CA005795 | DSP | c.3419del (p.Asp1140AlafsTer19) | ClinVar dbSNP |
6 | g.7579609A>C | CA362684010 | DSP | c.3419A>C (p.Asp1140Ala) |