Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583592_41583600delinsTGGTGCGCC | CA2260085469 | KRT14 | c.1004_1012delinsGGCGCACCA (p.Arg335=) n.454_462delinsGGCGCACCA | |
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 |
17 | g.41583598G>C | CA399476541 | KRT14 | c.1006C>G (p.Arg336Gly) n.456C>G | |
17 | g.41583598G= | CA2260085475 | KRT14 | c.1006C= (p.Arg336=) n.456C= | |
17 | g.41583598G>T | CA399476543 | KRT14 | c.1006C>A (p.Arg336Ser) n.456C>A | |
17 | g.41583599C>A | CA500205381 | KRT14 | c.1005G>T (p.Arg335=) n.455G>T | |
17 | g.41583599C>G | CA500205382 | KRT14 | c.1005G>C (p.Arg335=) n.455G>C | gnomAD v4 |
17 | g.41583599C>T | CA500205383 | KRT14 | c.1005G>A (p.Arg335=) n.455G>A | |
17 | g.41583600C>A | CA399476547 | KRT14 | c.1004G>T (p.Arg335Leu) n.454G>T | |
17 | g.41583600C= | CA2260085476 | KRT14 | c.1004G= (p.Arg335=) n.454G= | |
17 | g.41583600C>G | CA399476548 | KRT14 | c.1004G>C (p.Arg335Pro) n.454G>C | |
17 | g.41583600C>T | CA399476550 | KRT14 | c.1004G>A (p.Arg335Gln) n.454G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583601G>A | CA8562541 | KRT14 | c.1003C>T (p.Arg335Trp) n.453C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583601G>C | CA399476553 | KRT14 | c.1003C>G (p.Arg335Gly) n.453C>G | gnomAD v4 |
17 | g.41583601G= | CA2260085477 | KRT14 | c.1003C= (p.Arg335=) n.453C= | |
17 | g.41583601G>T | CA500205384 | KRT14 | c.1003C>A (p.Arg335=) n.453C>A | gnomAD v4 |
17 | g.41583602G>A | CA500205385 | KRT14 | c.1002C>T (p.Leu334=) n.452C>T | |
17 | g.41583602G>C | CA8562542 | KRT14 | c.1002C>G (p.Leu334=) n.452C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583602G= | CA2260085478 | KRT14 | c.1002C= (p.Leu334=) n.452C= | |
17 | g.41583602G>T | CA500205386 | KRT14 | c.1002C>A (p.Leu334=) n.452C>A | |
17 | g.41583603A>C | CA399476558 | KRT14 | c.1001T>G (p.Leu334Arg) n.451T>G | |
17 | g.41583603A>G | CA399476560 | KRT14 | c.1001T>C (p.Leu334Pro) n.451T>C | |
17 | g.41583603A>T | CA399476555 | KRT14 | c.1001T>A (p.Leu334His) n.451T>A | |
17 | g.41583604G>A | CA399476565 | KRT14 | c.1000C>T (p.Leu334Phe) n.450C>T | dbSNP gnomAD v4 |
17 | g.41583604G>C | CA399476563 | KRT14 | c.1000C>G (p.Leu334Val) n.450C>G | |
17 | g.41583604G= | CA2260085479 | KRT14 | c.1000C= (p.Leu334=) n.450C= | |
17 | g.41583604G>T | CA399476567 | KRT14 | c.1000C>A (p.Leu334Ile) n.450C>A | |
17 | g.41583605C>A | CA399476570 | KRT14 | c.999G>T (p.Glu333Asp) n.449G>T | |
17 | g.41583605C= | CA2260085480 | KRT14 | c.999G= (p.Glu333=) n.449G= | |
17 | g.41583605C>G | CA399476572 | KRT14 | c.999G>C (p.Glu333Asp) n.449G>C | |
17 | g.41583605C>T | CA500205387 | KRT14 | c.999G>A (p.Glu333=) n.449G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583606T>A | CA399476575 | KRT14 | c.998A>T (p.Glu333Val) n.448A>T | |
17 | g.41583606T>C | CA399476577 | KRT14 | c.998A>G (p.Glu333Gly) n.448A>G | |
17 | g.41583606T>G | CA399476579 | KRT14 | c.998A>C (p.Glu333Ala) n.448A>C |