Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583780C>ACA399477121KRT14c.907G>T (p.Glu303Ter)
n.357G>T
17g.41583780C=CA2260085566KRT14c.907G= (p.Glu303=)
n.357G=
17g.41583780C>GCA399477123KRT14c.907G>C (p.Glu303Gln)
n.357G>C
17g.41583780C>TCA399477125KRT14c.907G>A (p.Glu303Lys)
n.357G>A
ClinVar dbSNP gnomAD v4 COSMIC
17g.41583781G>ACA8562582KRT14c.906C>T (p.Ala302=)
n.356C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583781G>CCA500205442KRT14c.906C>G (p.Ala302=)
n.356C>G
17g.41583781G=CA2260085567KRT14c.906C= (p.Ala302=)
n.356C=
17g.41583781G>TCA500205444KRT14c.906C>A (p.Ala302=)
n.356C>A
gnomAD v4
17g.41583782G>ACA399477127KRT14c.905C>T (p.Ala302Val)
n.355C>T
17g.41583782G>CCA399477128KRT14c.905C>G (p.Ala302Gly)
n.355C>G
17g.41583782G>TCA399477130KRT14c.905C>A (p.Ala302Asp)
n.355C>A
17g.41583783C>ACA399477133KRT14c.904G>T (p.Ala302Ser)
n.354G>T
17g.41583783C>GCA399477134KRT14c.904G>C (p.Ala302Pro)
n.354G>C
17g.41583783C>TCA399477136KRT14c.904G>A (p.Ala302Thr)
n.354G>A
17g.41583784A>CCA399477138KRT14c.903T>G (p.Asp301Glu)
n.353T>G
17g.41583784A>GCA500205452KRT14c.903T>C (p.Asp301=)
n.353T>C
17g.41583784A>TCA399477140KRT14c.903T>A (p.Asp301Glu)
n.353T>A
17g.41583785T>ACA399477144KRT14c.902A>T (p.Asp301Val)
n.352A>T
17g.41583785T>CCA399477146KRT14c.902A>G (p.Asp301Gly)
n.352A>G
gnomAD v4
17g.41583785T>GCA399477148KRT14c.902A>C (p.Asp301Ala)
n.352A>C
17g.41583786C>ACA399477151KRT14c.901G>T (p.Asp301Tyr)
n.351G>T
17g.41583786C>GCA399477152KRT14c.901G>C (p.Asp301His)
n.351G>C
17g.41583786C>TCA399477154KRT14c.901G>A (p.Asp301Asn)
n.351G>A
17g.41583787C>ACA399477157KRT14c.900G>T (p.Lys300Asn)
n.350G>T
17g.41583787C=CA2260085568KRT14c.900G= (p.Lys300=)
n.350G=
17g.41583787C>GCA399477159KRT14c.900G>C (p.Lys300Asn)
n.350G>C
17g.41583787C>TCA290665011KRT14c.900G>A (p.Lys300=)
n.350G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583788T>ACA399477164KRT14c.899A>T (p.Lys300Met)
n.349A>T
17g.41583788T>CCA399477165KRT14c.899A>G (p.Lys300Arg)
n.349A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583788T>GCA399477166KRT14c.899A>C (p.Lys300Thr)
n.349A>C
17g.41583788T=CA2260085569KRT14c.899A= (p.Lys300=)
n.349A=
17g.41583789T>ACA399477169KRT14c.898A>T (p.Lys300Ter)
n.348A>T
17g.41583789T>CCA399477173KRT14c.898A>G (p.Lys300Glu)
n.348A>G
17g.41583789T>GCA399477170KRT14c.898A>C (p.Lys300Gln)
n.348A>C
17g.41583790G>ACA500205459KRT14c.897C>T (p.Arg299=)
n.347C>T
17g.41583790G>CCA500205461KRT14c.897C>G (p.Arg299=)
n.347C>G
17g.41583790G>TCA500205460KRT14c.897C>A (p.Arg299=)
n.347C>A
17g.41583791C>ACA399477176KRT14c.896G>T (p.Arg299Leu)
n.346G>T
dbSNP gnomAD v3 gnomAD v4
17g.41583791C=CA2260085570KRT14c.896G= (p.Arg299=)
n.346G=
17g.41583791C>GCA399477179KRT14c.896G>C (p.Arg299Pro)
n.346G>C
17g.41583791C>TCA8562583KRT14c.896G>A (p.Arg299His)
n.346G>A
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583792G>ACA399477184KRT14c.895C>T (p.Arg299Cys)
n.345C>T
dbSNP gnomAD v4
17g.41583792G>CCA399477186KRT14c.895C>G (p.Arg299Gly)
n.345C>G
17g.41583792G=CA2260085571KRT14c.895C= (p.Arg299=)
n.345C=
17g.41583792G>TCA399477189KRT14c.895C>A (p.Arg299Ser)
n.345C>A
17g.41583793G>ACA500205468KRT14c.894C>T (p.Asn298=)
n.344C>T
gnomAD v4
17g.41583793G>CCA399477191KRT14c.894C>G (p.Asn298Lys)
n.344C>G
17g.41583793G>TCA399477192KRT14c.894C>A (p.Asn298Lys)
n.344C>A
17g.41583794T>ACA399477196KRT14c.893A>T (p.Asn298Ile)
n.343A>T
17g.41583794T>CCA399477198KRT14c.893A>G (p.Asn298Ser)
n.343A>G

Number of alleles fetched