Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583585T>A | CA399476463 | KRT14 | c.1019A>T (p.Asn340Ile) n.469A>T | dbSNP gnomAD v4 |
17 | g.41583585T>C | CA399476465 | KRT14 | c.1019A>G (p.Asn340Ser) n.469A>G | gnomAD v4 |
17 | g.41583585T>G | CA399476468 | KRT14 | c.1019A>C (p.Asn340Thr) n.469A>C | dbSNP |
17 | g.41583585T= | CA2260085465 | KRT14 | c.1019A= (p.Asn340=) n.469A= | |
17 | g.41583586T>A | CA399476471 | KRT14 | c.1018A>T (p.Asn340Tyr) n.468A>T | |
17 | g.41583586T>C | CA399476473 | KRT14 | c.1018A>G (p.Asn340Asp) n.468A>G | |
17 | g.41583586T>G | CA399476475 | KRT14 | c.1018A>C (p.Asn340His) n.468A>C | |
17 | g.41583587C>A | CA399476478 | KRT14 | c.1017G>T (p.Gln339His) n.467G>T | |
17 | g.41583587C>G | CA399476480 | KRT14 | c.1017G>C (p.Gln339His) n.467G>C | |
17 | g.41583587C>T | CA500205375 | KRT14 | c.1017G>A (p.Gln339=) n.467G>A | |
17 | g.41583588T>A | CA399476483 | KRT14 | c.1016A>T (p.Gln339Leu) n.466A>T | |
17 | g.41583588T>C | CA399476484 | KRT14 | c.1016A>G (p.Gln339Arg) n.466A>G | |
17 | g.41583588T>G | CA399476486 | KRT14 | c.1016A>C (p.Gln339Pro) n.466A>C | |
17 | g.41583589G>A | CA399476492 | KRT14 | c.1015C>T (p.Gln339Ter) n.465C>T | |
17 | g.41583589G>C | CA399476490 | KRT14 | c.1015C>G (p.Gln339Glu) n.465C>G | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583589G= | CA2260085466 | KRT14 | c.1015C= (p.Gln339=) n.465C= | |
17 | g.41583589G>T | CA399476489 | KRT14 | c.1015C>A (p.Gln339Lys) n.465C>A | |
17 | g.41583590C>A | CA399476496 | KRT14 | c.1014G>T (p.Met338Ile) n.464G>T | |
17 | g.41583590C= | CA2260085467 | KRT14 | c.1014G= (p.Met338=) n.464G= | |
17 | g.41583590C>G | CA399476498 | KRT14 | c.1014G>C (p.Met338Ile) n.464G>C | gnomAD v4 |
17 | g.41583590C>T | CA399476500 | KRT14 | c.1014G>A (p.Met338Ile) n.464G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583591A= | CA2260085468 | KRT14 | c.1013T= (p.Met338=) n.463T= | |
17 | g.41583591A>C | CA8562536 | KRT14 | c.1013T>G (p.Met338Arg) n.463T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583591A>G | CA8562537 | KRT14 | c.1013T>C (p.Met338Thr) n.463T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583591A>T | CA399476507 | KRT14 | c.1013T>A (p.Met338Lys) n.463T>A | |
17 | g.41583592T>A | CA399476511 | KRT14 | c.1012A>T (p.Met338Leu) n.462A>T | |
17 | g.41583592T>C | CA399476513 | KRT14 | c.1012A>G (p.Met338Val) n.462A>G | dbSNP |
17 | g.41583592T>G | CA399476515 | KRT14 | c.1012A>C (p.Met338Leu) n.462A>C | |
17 | g.41583592_41583600delinsTGGTGCGCC | CA2260085469 | KRT14 | c.1004_1012delinsGGCGCACCA (p.Arg335=) n.454_462delinsGGCGCACCA | |
17 | g.41583593G>A | CA500205377 | KRT14 | c.1011C>T (p.Thr337=) n.461C>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583593G>C | CA8562538 | KRT14 | c.1011C>G (p.Thr337=) n.461C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583593G= | CA2260085471 | KRT14 | c.1011C= (p.Thr337=) n.461C= | |
17 | g.41583593G>T | CA500205376 | KRT14 | c.1011C>A (p.Thr337=) n.461C>A | |
17 | g.41583595_41583602del | CA2260085470 | KRT14 | c.1004_1011del (p.Arg335HisfsTer7) n.454_461del | dbSNP |
17 | g.41583594G>A | CA399476520 | KRT14 | c.1010C>T (p.Thr337Ile) n.460C>T | COSMIC |
17 | g.41583594G>C | CA399476523 | KRT14 | c.1010C>G (p.Thr337Ser) n.460C>G | |
17 | g.41583594G>T | CA399476526 | KRT14 | c.1010C>A (p.Thr337Asn) n.460C>A | |
17 | g.41583595T>A | CA399476533 | KRT14 | c.1009A>T (p.Thr337Ser) n.459A>T | COSMIC |
17 | g.41583595T>C | CA399476529 | KRT14 | c.1009A>G (p.Thr337Ala) n.459A>G | dbSNP gnomAD v4 |
17 | g.41583595T>G | CA399476531 | KRT14 | c.1009A>C (p.Thr337Pro) n.459A>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583595T= | CA2260085472 | KRT14 | c.1009A= (p.Thr337=) n.459A= | |
17 | g.41583596G>A | CA500205378 | KRT14 | c.1008C>T (p.Arg336=) n.458C>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583596G>C | CA500205379 | KRT14 | c.1008C>G (p.Arg336=) n.458C>G | |
17 | g.41583596G= | CA2260085473 | KRT14 | c.1008C= (p.Arg336=) n.458C= | |
17 | g.41583596G>T | CA500205380 | KRT14 | c.1008C>A (p.Arg336=) n.458C>A | |
17 | g.41583597C>A | CA399476534 | KRT14 | c.1007G>T (p.Arg336Leu) n.457G>T | |
17 | g.41583597C= | CA2260085474 | KRT14 | c.1007G= (p.Arg336=) n.457G= | |
17 | g.41583597C>G | CA399476536 | KRT14 | c.1007G>C (p.Arg336Pro) n.457G>C | dbSNP |
17 | g.41583597C>T | CA8562539 | KRT14 | c.1007G>A (p.Arg336His) n.457G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.41583598G>A | CA8562540 | KRT14 | c.1006C>T (p.Arg336Cys) n.456C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |