Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41583093C>A | CA399474811 | KRT14 | c.1321+1G>T (n.1321+1G>T) n.269G>T | |
17 | g.41583093C= | CA2260085213 | KRT14 | c.1321+1G= (n.1321+1G=) n.269G= | |
17 | g.41583093C>G | CA399474816 | KRT14 | c.1321+1G>C (n.1321+1G>C) n.269G>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41583093C>T | CA399474814 | KRT14 | c.1321+1G>A (n.1321+1G>A) n.269G>A | gnomAD v4 |
17 | g.41583093_41583094delinsTT | CA645584609 | KRT14 | c.1321_1321+1delinsAA n.268_269delinsAA | COSMIC |
17 | g.41583094C>A | CA399474818 | KRT14 | c.1321G>T (p.Val441Leu) n.268G>T | dbSNP gnomAD v4 |
17 | g.41583094C= | CA2260085214 | KRT14 | c.1321G= (p.Val441=) n.268G= | |
17 | g.41583094C>G | CA399474821 | KRT14 | c.1321G>C (p.Val441Leu) n.268G>C | |
17 | g.41583094C>T | CA399474823 | KRT14 | c.1321G>A (p.Val441Met) n.268G>A | COSMIC |
17 | g.41583095A= | CA2260085215 | KRT14 | c.1320T= (p.Asp440=) n.267T= | |
17 | g.41583095A>C | CA399474825 | KRT14 | c.1320T>G (p.Asp440Glu) n.267T>G | |
17 | g.41583095A>G | CA8562412 | KRT14 | c.1320T>C (p.Asp440=) n.267T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.41583095A>T | CA399474840 | KRT14 | c.1320T>A (p.Asp440Glu) n.267T>A | gnomAD v4 |
17 | g.41583096T>A | CA399474843 | KRT14 | c.1319A>T (p.Asp440Val) n.266A>T | |
17 | g.41583096T>C | CA399474845 | KRT14 | c.1319A>G (p.Asp440Gly) n.266A>G | |
17 | g.41583096T>G | CA399474848 | KRT14 | c.1319A>C (p.Asp440Ala) n.266A>C | |
17 | g.41583097C>A | CA399474852 | KRT14 | c.1318G>T (p.Asp440Tyr) n.265G>T | |
17 | g.41583097C>G | CA399474854 | KRT14 | c.1318G>C (p.Asp440His) n.265G>C | |
17 | g.41583097C>T | CA399474856 | KRT14 | c.1318G>A (p.Asp440Asn) n.265G>A | |
17 | g.41583098T>A | CA399474859 | KRT14 | c.1317A>T (p.Arg439Ser) n.264A>T | |
17 | g.41583098T>C | CA500205033 | KRT14 | c.1317A>G (p.Arg439=) n.264A>G | |
17 | g.41583098T>G | CA399474860 | KRT14 | c.1317A>C (p.Arg439Ser) n.264A>C | |
17 | g.41583099C>A | CA399474864 | KRT14 | c.1316G>T (p.Arg439Ile) n.263G>T | |
17 | g.41583099C= | CA2260085216 | KRT14 | c.1316G= (p.Arg439=) n.263G= | |
17 | g.41583099C>G | CA399474866 | KRT14 | c.1316G>C (p.Arg439Thr) n.263G>C | dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.41583099C>T | CA399474868 | KRT14 | c.1316G>A (p.Arg439Lys) n.263G>A | |
17 | g.41583100T>A | CA399474869 | KRT14 | c.1315A>T (p.Arg439Ter) n.262A>T | |
17 | g.41583100T>C | CA399474871 | KRT14 | c.1315A>G (p.Arg439Gly) n.262A>G | |
17 | g.41583100T>G | CA500205038 | KRT14 | c.1315A>C (p.Arg439=) n.262A>C | |
17 | g.41583101G>A | CA500205041 | KRT14 | c.1314C>T (p.Ser438=) n.261C>T | |
17 | g.41583101G>C | CA500205045 | KRT14 | c.1314C>G (p.Ser438=) n.261C>G | |
17 | g.41583101G>T | CA500205046 | KRT14 | c.1314C>A (p.Ser438=) n.261C>A | |
17 | g.41583102G>A | CA399474873 | KRT14 | c.1313C>T (p.Ser438Phe) n.260C>T | |
17 | g.41583102G>C | CA399474874 | KRT14 | c.1313C>G (p.Ser438Cys) n.260C>G | |
17 | g.41583102G>T | CA399474877 | KRT14 | c.1313C>A (p.Ser438Tyr) n.260C>A | |
17 | g.41583103A>C | CA399474881 | KRT14 | c.1312T>G (p.Ser438Ala) n.259T>G | |
17 | g.41583103A>G | CA399474884 | KRT14 | c.1312T>C (p.Ser438Pro) n.259T>C | gnomAD v4 |
17 | g.41583103A>T | CA399474886 | KRT14 | c.1312T>A (p.Ser438Thr) n.259T>A | |
17 | g.41583104T>A | CA500205047 | KRT14 | c.1311A>T (p.Ser437=) n.258A>T | |
17 | g.41583104T>C | CA500205048 | KRT14 | c.1311A>G (p.Ser437=) n.258A>G | |
17 | g.41583104T>G | CA500205049 | KRT14 | c.1311A>C (p.Ser437=) n.258A>C | |
17 | g.41583105G>A | CA399474892 | KRT14 | c.1310C>T (p.Ser437Leu) n.257C>T | |
17 | g.41583105G>C | CA399474894 | KRT14 | c.1310C>G (p.Ser437Ter) n.257C>G | |
17 | g.41583105G>T | CA399474889 | KRT14 | c.1310C>A (p.Ser437Ter) n.257C>A | |
17 | g.41583106A>C | CA399474898 | KRT14 | c.1309T>G (p.Ser437Ala) n.256T>G | |
17 | g.41583106A>G | CA399474900 | KRT14 | c.1309T>C (p.Ser437Pro) n.256T>C | |
17 | g.41583106A>T | CA399474902 | KRT14 | c.1309T>A (p.Ser437Thr) n.256T>A | |
17 | g.41583107C>A | CA399474905 | KRT14 | c.1308G>T (p.Gln436His) n.255G>T | |
17 | g.41583107C>G | CA399474907 | KRT14 | c.1308G>C (p.Gln436His) n.255G>C | gnomAD v4 |
17 | g.41583107C>T | CA500205053 | KRT14 | c.1308G>A (p.Gln436=) n.255G>A |