Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583573T>A | CA399476397 | KRT14 | c.1031A>T (p.Glu344Val) n.481A>T | |
17 | g.41583573T>C | CA399476398 | KRT14 | c.1031A>G (p.Glu344Gly) n.481A>G | |
17 | g.41583573T>G | CA399476401 | KRT14 | c.1031A>C (p.Glu344Ala) n.481A>C | |
17 | g.41583574C>A | CA399476403 | KRT14 | c.1030G>T (p.Glu344Ter) n.480G>T | |
17 | g.41583574C= | CA2260085461 | KRT14 | c.1030G= (p.Glu344=) n.480G= | |
17 | g.41583574C>G | CA399476406 | KRT14 | c.1030G>C (p.Glu344Gln) n.480G>C | |
17 | g.41583574C>T | CA399476407 | KRT14 | c.1030G>A (p.Glu344Lys) n.480G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583575A>C | CA399476410 | KRT14 | c.1029T>G (p.Ile343Met) n.479T>G | |
17 | g.41583575A>G | CA500205367 | KRT14 | c.1029T>C (p.Ile343=) n.479T>C | gnomAD v4 |
17 | g.41583575A>T | CA500205368 | KRT14 | c.1029T>A (p.Ile343=) n.479T>A | |
17 | g.41583576A>C | CA399476415 | KRT14 | c.1028T>G (p.Ile343Ser) n.478T>G | |
17 | g.41583576A>G | CA399476418 | KRT14 | c.1028T>C (p.Ile343Thr) n.478T>C | gnomAD v4 |
17 | g.41583576A>T | CA399476413 | KRT14 | c.1028T>A (p.Ile343Asn) n.478T>A | |
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 |