Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583577T>A | CA399476424 | KRT14 | c.1027A>T (p.Ile343Phe) n.477A>T | |
17 | g.41583577T>C | CA399476421 | KRT14 | c.1027A>G (p.Ile343Val) n.477A>G | |
17 | g.41583577T>G | CA399476426 | KRT14 | c.1027A>C (p.Ile343Leu) n.477A>C | |
17 | g.41583578C>A | CA399476428 | KRT14 | c.1026G>T (p.Glu342Asp) n.476G>T | |
17 | g.41583578C>G | CA399476429 | KRT14 | c.1026G>C (p.Glu342Asp) n.476G>C | |
17 | g.41583578C>T | CA500205369 | KRT14 | c.1026G>A (p.Glu342=) n.476G>A | |
17 | g.41583579T>A | CA399476433 | KRT14 | c.1025A>T (p.Glu342Val) n.475A>T | |
17 | g.41583579T>C | CA399476435 | KRT14 | c.1025A>G (p.Glu342Gly) n.475A>G | |
17 | g.41583579T>G | CA399476438 | KRT14 | c.1025A>C (p.Glu342Ala) n.475A>C | |
17 | g.41583580C>A | CA399476440 | KRT14 | c.1024G>T (p.Glu342Ter) n.474G>T | |
17 | g.41583580C= | CA2260085462 | KRT14 | c.1024G= (p.Glu342=) n.474G= | |
17 | g.41583580C>G | CA399476442 | KRT14 | c.1024G>C (p.Glu342Gln) n.474G>C | |
17 | g.41583580C>T | CA399476444 | KRT14 | c.1024G>A (p.Glu342Lys) n.474G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.41583581C>A | CA500205370 | KRT14 | c.1023G>T (p.Leu341=) n.473G>T | |
17 | g.41583581C>G | CA500205371 | KRT14 | c.1023G>C (p.Leu341=) n.473G>C | gnomAD v4 |
17 | g.41583581C>T | CA500205372 | KRT14 | c.1023G>A (p.Leu341=) n.473G>A | |
17 | g.41583582A>C | CA399476447 | KRT14 | c.1022T>G (p.Leu341Arg) n.472T>G | |
17 | g.41583582A>G | CA399476449 | KRT14 | c.1022T>C (p.Leu341Pro) n.472T>C | |
17 | g.41583582A>T | CA399476452 | KRT14 | c.1022T>A (p.Leu341Gln) n.472T>A | |
17 | g.41583583G>A | CA500205373 | KRT14 | c.1021C>T (p.Leu341=) n.471C>T | dbSNP gnomAD v4 |
17 | g.41583583G>C | CA8562534 | KRT14 | c.1021C>G (p.Leu341Val) n.471C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583583G= | CA2260085463 | KRT14 | c.1021C= (p.Leu341=) n.471C= | |
17 | g.41583583G>T | CA399476456 | KRT14 | c.1021C>A (p.Leu341Met) n.471C>A | dbSNP gnomAD v4 |
17 | g.41583584G>A | CA500205374 | KRT14 | c.1020C>T (p.Asn340=) n.470C>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583584G>C | CA399476459 | KRT14 | c.1020C>G (p.Asn340Lys) n.470C>G | |
17 | g.41583584G= | CA2260085464 | KRT14 | c.1020C= (p.Asn340=) n.470C= | |
17 | g.41583584G>T | CA8562535 | KRT14 | c.1020C>A (p.Asn340Lys) n.470C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
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 |