Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583592_41583600delinsTGGTGCGCCCA2260085469KRT14c.1004_1012delinsGGCGCACCA (p.Arg335=)
n.454_462delinsGGCGCACCA
17g.41583595_41583602delCA2260085470KRT14c.1004_1011del (p.Arg335HisfsTer7)
n.454_461del
dbSNP
17g.41583594G>ACA399476520KRT14c.1010C>T (p.Thr337Ile)
n.460C>T
COSMIC
17g.41583594G>CCA399476523KRT14c.1010C>G (p.Thr337Ser)
n.460C>G
17g.41583594G>TCA399476526KRT14c.1010C>A (p.Thr337Asn)
n.460C>A
17g.41583595T>ACA399476533KRT14c.1009A>T (p.Thr337Ser)
n.459A>T
COSMIC
17g.41583595T>CCA399476529KRT14c.1009A>G (p.Thr337Ala)
n.459A>G
dbSNP gnomAD v4
17g.41583595T>GCA399476531KRT14c.1009A>C (p.Thr337Pro)
n.459A>C
dbSNP gnomAD v2 gnomAD v4
17g.41583595T=CA2260085472KRT14c.1009A= (p.Thr337=)
n.459A=
17g.41583596G>ACA500205378KRT14c.1008C>T (p.Arg336=)
n.458C>T
dbSNP gnomAD v3 gnomAD v4
17g.41583596G>CCA500205379KRT14c.1008C>G (p.Arg336=)
n.458C>G
17g.41583596G=CA2260085473KRT14c.1008C= (p.Arg336=)
n.458C=
17g.41583596G>TCA500205380KRT14c.1008C>A (p.Arg336=)
n.458C>A
17g.41583597C>ACA399476534KRT14c.1007G>T (p.Arg336Leu)
n.457G>T
17g.41583597C=CA2260085474KRT14c.1007G= (p.Arg336=)
n.457G=
17g.41583597C>GCA399476536KRT14c.1007G>C (p.Arg336Pro)
n.457G>C
dbSNP
17g.41583597C>TCA8562539KRT14c.1007G>A (p.Arg336His)
n.457G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41583598G>ACA8562540KRT14c.1006C>T (p.Arg336Cys)
n.456C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583598G>CCA399476541KRT14c.1006C>G (p.Arg336Gly)
n.456C>G
17g.41583598G=CA2260085475KRT14c.1006C= (p.Arg336=)
n.456C=
17g.41583598G>TCA399476543KRT14c.1006C>A (p.Arg336Ser)
n.456C>A
17g.41583599C>ACA500205381KRT14c.1005G>T (p.Arg335=)
n.455G>T
17g.41583599C>GCA500205382KRT14c.1005G>C (p.Arg335=)
n.455G>C
gnomAD v4
17g.41583599C>TCA500205383KRT14c.1005G>A (p.Arg335=)
n.455G>A
17g.41583600C>ACA399476547KRT14c.1004G>T (p.Arg335Leu)
n.454G>T
17g.41583600C=CA2260085476KRT14c.1004G= (p.Arg335=)
n.454G=
17g.41583600C>GCA399476548KRT14c.1004G>C (p.Arg335Pro)
n.454G>C
17g.41583600C>TCA399476550KRT14c.1004G>A (p.Arg335Gln)
n.454G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583601G>ACA8562541KRT14c.1003C>T (p.Arg335Trp)
n.453C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583601G>CCA399476553KRT14c.1003C>G (p.Arg335Gly)
n.453C>G
gnomAD v4
17g.41583601G=CA2260085477KRT14c.1003C= (p.Arg335=)
n.453C=
17g.41583601G>TCA500205384KRT14c.1003C>A (p.Arg335=)
n.453C>A
gnomAD v4
17g.41583602G>ACA500205385KRT14c.1002C>T (p.Leu334=)
n.452C>T
17g.41583602G>CCA8562542KRT14c.1002C>G (p.Leu334=)
n.452C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583602G=CA2260085478KRT14c.1002C= (p.Leu334=)
n.452C=
17g.41583602G>TCA500205386KRT14c.1002C>A (p.Leu334=)
n.452C>A
17g.41583603A>CCA399476558KRT14c.1001T>G (p.Leu334Arg)
n.451T>G
17g.41583603A>GCA399476560KRT14c.1001T>C (p.Leu334Pro)
n.451T>C
17g.41583603A>TCA399476555KRT14c.1001T>A (p.Leu334His)
n.451T>A
17g.41583604G>ACA399476565KRT14c.1000C>T (p.Leu334Phe)
n.450C>T
dbSNP gnomAD v4
17g.41583604G>CCA399476563KRT14c.1000C>G (p.Leu334Val)
n.450C>G
17g.41583604G=CA2260085479KRT14c.1000C= (p.Leu334=)
n.450C=
17g.41583604G>TCA399476567KRT14c.1000C>A (p.Leu334Ile)
n.450C>A
17g.41583605C>ACA399476570KRT14c.999G>T (p.Glu333Asp)
n.449G>T
17g.41583605C=CA2260085480KRT14c.999G= (p.Glu333=)
n.449G=
17g.41583605C>GCA399476572KRT14c.999G>C (p.Glu333Asp)
n.449G>C
17g.41583605C>TCA500205387KRT14c.999G>A (p.Glu333=)
n.449G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583606T>ACA399476575KRT14c.998A>T (p.Glu333Val)
n.448A>T
17g.41583606T>CCA399476577KRT14c.998A>G (p.Glu333Gly)
n.448A>G
17g.41583606T>GCA399476579KRT14c.998A>C (p.Glu333Ala)
n.448A>C

Number of alleles fetched