Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583093C>ACA399474811KRT14c.1321+1G>T (n.1321+1G>T)
n.269G>T
17g.41583093C=CA2260085213KRT14c.1321+1G= (n.1321+1G=)
n.269G=
17g.41583093C>GCA399474816KRT14c.1321+1G>C (n.1321+1G>C)
n.269G>C
dbSNP gnomAD v3 gnomAD v4
17g.41583093C>TCA399474814KRT14c.1321+1G>A (n.1321+1G>A)
n.269G>A
gnomAD v4
17g.41583093_41583094delinsTTCA645584609KRT14c.1321_1321+1delinsAA
n.268_269delinsAA
COSMIC
17g.41583094C>ACA399474818KRT14c.1321G>T (p.Val441Leu)
n.268G>T
dbSNP gnomAD v4
17g.41583094C=CA2260085214KRT14c.1321G= (p.Val441=)
n.268G=
17g.41583094C>GCA399474821KRT14c.1321G>C (p.Val441Leu)
n.268G>C
17g.41583094C>TCA399474823KRT14c.1321G>A (p.Val441Met)
n.268G>A
COSMIC
17g.41583095A=CA2260085215KRT14c.1320T= (p.Asp440=)
n.267T=
17g.41583095A>CCA399474825KRT14c.1320T>G (p.Asp440Glu)
n.267T>G
17g.41583095A>GCA8562412KRT14c.1320T>C (p.Asp440=)
n.267T>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583095A>TCA399474840KRT14c.1320T>A (p.Asp440Glu)
n.267T>A
gnomAD v4
17g.41583096T>ACA399474843KRT14c.1319A>T (p.Asp440Val)
n.266A>T
17g.41583096T>CCA399474845KRT14c.1319A>G (p.Asp440Gly)
n.266A>G
17g.41583096T>GCA399474848KRT14c.1319A>C (p.Asp440Ala)
n.266A>C
17g.41583097C>ACA399474852KRT14c.1318G>T (p.Asp440Tyr)
n.265G>T
17g.41583097C>GCA399474854KRT14c.1318G>C (p.Asp440His)
n.265G>C
17g.41583097C>TCA399474856KRT14c.1318G>A (p.Asp440Asn)
n.265G>A
17g.41583098T>ACA399474859KRT14c.1317A>T (p.Arg439Ser)
n.264A>T
17g.41583098T>CCA500205033KRT14c.1317A>G (p.Arg439=)
n.264A>G
17g.41583098T>GCA399474860KRT14c.1317A>C (p.Arg439Ser)
n.264A>C
17g.41583099C>ACA399474864KRT14c.1316G>T (p.Arg439Ile)
n.263G>T
17g.41583099C=CA2260085216KRT14c.1316G= (p.Arg439=)
n.263G=
17g.41583099C>GCA399474866KRT14c.1316G>C (p.Arg439Thr)
n.263G>C
dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.41583099C>TCA399474868KRT14c.1316G>A (p.Arg439Lys)
n.263G>A
17g.41583100T>ACA399474869KRT14c.1315A>T (p.Arg439Ter)
n.262A>T
17g.41583100T>CCA399474871KRT14c.1315A>G (p.Arg439Gly)
n.262A>G
17g.41583100T>GCA500205038KRT14c.1315A>C (p.Arg439=)
n.262A>C
17g.41583101G>ACA500205041KRT14c.1314C>T (p.Ser438=)
n.261C>T
17g.41583101G>CCA500205045KRT14c.1314C>G (p.Ser438=)
n.261C>G
17g.41583101G>TCA500205046KRT14c.1314C>A (p.Ser438=)
n.261C>A
17g.41583102G>ACA399474873KRT14c.1313C>T (p.Ser438Phe)
n.260C>T
17g.41583102G>CCA399474874KRT14c.1313C>G (p.Ser438Cys)
n.260C>G
17g.41583102G>TCA399474877KRT14c.1313C>A (p.Ser438Tyr)
n.260C>A
17g.41583103A>CCA399474881KRT14c.1312T>G (p.Ser438Ala)
n.259T>G
17g.41583103A>GCA399474884KRT14c.1312T>C (p.Ser438Pro)
n.259T>C
gnomAD v4
17g.41583103A>TCA399474886KRT14c.1312T>A (p.Ser438Thr)
n.259T>A
17g.41583104T>ACA500205047KRT14c.1311A>T (p.Ser437=)
n.258A>T
17g.41583104T>CCA500205048KRT14c.1311A>G (p.Ser437=)
n.258A>G
17g.41583104T>GCA500205049KRT14c.1311A>C (p.Ser437=)
n.258A>C
17g.41583105G>ACA399474892KRT14c.1310C>T (p.Ser437Leu)
n.257C>T
17g.41583105G>CCA399474894KRT14c.1310C>G (p.Ser437Ter)
n.257C>G
17g.41583105G>TCA399474889KRT14c.1310C>A (p.Ser437Ter)
n.257C>A
17g.41583106A>CCA399474898KRT14c.1309T>G (p.Ser437Ala)
n.256T>G
17g.41583106A>GCA399474900KRT14c.1309T>C (p.Ser437Pro)
n.256T>C
17g.41583106A>TCA399474902KRT14c.1309T>A (p.Ser437Thr)
n.256T>A
17g.41583107C>ACA399474905KRT14c.1308G>T (p.Gln436His)
n.255G>T
17g.41583107C>GCA399474907KRT14c.1308G>C (p.Gln436His)
n.255G>C
gnomAD v4
17g.41583107C>TCA500205053KRT14c.1308G>A (p.Gln436=)
n.255G>A

Number of alleles fetched