Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
17 | g.41583607C>A | CA399476581 | KRT14 | c.997G>T (p.Glu333Ter) n.447G>T | |
17 | g.41583607C= | CA2260085481 | KRT14 | c.997G= (p.Glu333=) n.447G= | |
17 | g.41583607C>G | CA399476583 | KRT14 | c.997G>C (p.Glu333Gln) n.447G>C | dbSNP gnomAD v4 |
17 | g.41583607C>T | CA399476585 | KRT14 | c.997G>A (p.Glu333Lys) n.447G>A | |
17 | g.41583608C>A | CA500205388 | KRT14 | c.996G>T (p.Ser332=) n.446G>T | |
17 | g.41583608C= | CA2260085482 | KRT14 | c.996G= (p.Ser332=) n.446G= | |
17 | g.41583608C>G | CA500205389 | KRT14 | c.996G>C (p.Ser332=) n.446G>C | |
17 | g.41583608C>T | CA8562543 | KRT14 | c.996G>A (p.Ser332=) n.446G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583609G>A | CA8562544 | KRT14 | c.995C>T (p.Ser332Leu) n.445C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41583609G>C | CA399476591 | KRT14 | c.995C>G (p.Ser332Trp) n.445C>G | |
17 | g.41583609G= | CA2260085483 | KRT14 | c.995C= (p.Ser332=) n.445C= | |
17 | g.41583609G>T | CA399476593 | KRT14 | c.995C>A (p.Ser332Ter) n.445C>A | gnomAD v4 |
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 |