Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583610A>C | CA399476601 | KRT14 | c.994T>G (p.Ser332Ala) n.444T>G | |
17 | g.41583610A>G | CA399476598 | KRT14 | c.994T>C (p.Ser332Pro) n.444T>C | |
17 | g.41583610A>T | CA399476596 | KRT14 | c.994T>A (p.Ser332Thr) n.444T>A | gnomAD v4 |
17 | g.41583611G>A | CA500205390 | KRT14 | c.993C>T (p.Ile331=) n.443C>T | |
17 | g.41583611G>C | CA399476603 | KRT14 | c.993C>G (p.Ile331Met) n.443C>G | |
17 | g.41583611G= | CA2260085484 | KRT14 | c.993C= (p.Ile331=) n.443C= | |
17 | g.41583611G>T | CA500205391 | KRT14 | c.993C>A (p.Ile331=) n.443C>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.41583612A>C | CA399476605 | KRT14 | c.992T>G (p.Ile331Ser) n.442T>G | |
17 | g.41583612A>G | CA399476607 | KRT14 | c.992T>C (p.Ile331Thr) n.442T>C | |
17 | g.41583612A>T | CA399476609 | KRT14 | c.992T>A (p.Ile331Asn) n.442T>A | |
17 | g.41583613T>A | CA399476613 | KRT14 | c.991A>T (p.Ile331Phe) n.441A>T | |
17 | g.41583613T>C | CA399476615 | KRT14 | c.991A>G (p.Ile331Val) n.441A>G | gnomAD v4 |
17 | g.41583613T>G | CA8562545 | KRT14 | c.991A>C (p.Ile331Leu) n.441A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583613T= | CA2260085485 | KRT14 | c.991A= (p.Ile331=) n.441A= | |
17 | g.41583614C>A | CA399476620 | KRT14 | c.990G>T (p.Glu330Asp) n.440G>T | |
17 | g.41583614C>G | CA399476622 | KRT14 | c.990G>C (p.Glu330Asp) n.440G>C | |
17 | g.41583614C>T | CA500205392 | KRT14 | c.990G>A (p.Glu330=) n.440G>A | |
17 | g.41583615T>A | CA399476625 | KRT14 | c.989A>T (p.Glu330Val) n.439A>T | |
17 | g.41583615T>C | CA399476627 | KRT14 | c.989A>G (p.Glu330Gly) n.439A>G | |
17 | g.41583615T>G | CA8562546 | KRT14 | c.989A>C (p.Glu330Ala) n.439A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583615T= | CA2260085486 | KRT14 | c.989A= (p.Glu330=) n.439A= | |
17 | g.41583616C>A | CA399476633 | KRT14 | c.988G>T (p.Glu330Ter) n.438G>T | |
17 | g.41583616C= | CA2260085487 | KRT14 | c.988G= (p.Glu330=) n.438G= | |
17 | g.41583616C>G | CA399476630 | KRT14 | c.988G>C (p.Glu330Gln) n.438G>C | |
17 | g.41583616C>T | CA8562547 | KRT14 | c.988G>A (p.Glu330Lys) n.438G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583617G>A | CA8562548 | KRT14 | c.987C>T (p.Ser329=) n.437C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583617G>C | CA399476639 | KRT14 | c.987C>G (p.Ser329Arg) n.437C>G | gnomAD v4 |
17 | g.41583617G= | CA2260085488 | KRT14 | c.987C= (p.Ser329=) n.437C= | |
17 | g.41583617G>T | CA399476636 | KRT14 | c.987C>A (p.Ser329Arg) n.437C>A | dbSNP gnomAD v4 |
17 | g.41583618C>A | CA399476641 | KRT14 | c.986G>T (p.Ser329Ile) n.436G>T | |
17 | g.41583618C= | CA2260085489 | KRT14 | c.986G= (p.Ser329=) n.436G= | |
17 | g.41583618C>G | CA399476642 | KRT14 | c.986G>C (p.Ser329Thr) n.436G>C | gnomAD v4 |
17 | g.41583618C>T | CA399476644 | KRT14 | c.986G>A (p.Ser329Asn) n.436G>A | dbSNP |
17 | g.41583619T>A | CA399476647 | KRT14 | c.985A>T (p.Ser329Cys) n.435A>T | |
17 | g.41583619T>C | CA399476649 | KRT14 | c.985A>G (p.Ser329Gly) n.435A>G | gnomAD v4 |
17 | g.41583619T>G | CA399476651 | KRT14 | c.985A>C (p.Ser329Arg) n.435A>C | |
17 | g.41583620C>A | CA399476652 | KRT14 | c.984G>T (p.Lys328Asn) n.434G>T | |
17 | g.41583620C>G | CA399476654 | KRT14 | c.984G>C (p.Lys328Asn) n.434G>C | |
17 | g.41583620C>T | CA500205393 | KRT14 | c.984G>A (p.Lys328=) n.434G>A | ClinVar |
17 | g.41583621T>A | CA399476659 | KRT14 | c.983A>T (p.Lys328Met) n.433A>T | |
17 | g.41583621T>C | CA399476660 | KRT14 | c.983A>G (p.Lys328Arg) n.433A>G | |
17 | g.41583621T>G | CA399476663 | KRT14 | c.983A>C (p.Lys328Thr) n.433A>C | |
17 | g.41583622T>A | CA399476671 | KRT14 | c.982A>T (p.Lys328Ter) n.432A>T | |
17 | g.41583622T>C | CA399476669 | KRT14 | c.982A>G (p.Lys328Glu) n.432A>G | |
17 | g.41583622T>G | CA399476667 | KRT14 | c.982A>C (p.Lys328Gln) n.432A>C | |
17 | g.41583623G>A | CA500205394 | KRT14 | c.981C>T (p.Gly327=) n.431C>T | |
17 | g.41583623G>C | CA500205395 | KRT14 | c.981C>G (p.Gly327=) n.431C>G | gnomAD v4 |
17 | g.41583623G>T | CA500205396 | KRT14 | c.981C>A (p.Gly327=) n.431C>A | |
17 | g.41583624C>A | CA399476673 | KRT14 | c.980G>T (p.Gly327Val) n.430G>T | |
17 | g.41583624C>G | CA399476675 | KRT14 | c.980G>C (p.Gly327Ala) n.430G>C |