Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47448079G>ACA474430514RAPSNc.264C>T (p.Asn88=)
11g.47448079G>CCA380334837RAPSNc.264C>G (p.Asn88Lys)
11g.47448079G=CA1969378565RAPSNc.264C= (p.Asn88=)
11g.47448079G>TCA199511RAPSNc.264C>A (p.Asn88Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.47448080T>ACA380334845RAPSNc.263A>T (p.Asn88Ile)
11g.47448080T>CCA380334850RAPSNc.263A>G (p.Asn88Ser)
dbSNP
11g.47448080T>GCA380334851RAPSNc.263A>C (p.Asn88Thr)
11g.47448080T=CA1969378570RAPSNc.263A= (p.Asn88=)
11g.47448081T>ACA380334854RAPSNc.262A>T (p.Asn88Tyr)
11g.47448081T>CCA380334855RAPSNc.262A>G (p.Asn88Asp)
11g.47448081T>GCA380334857RAPSNc.262A>C (p.Asn88His)
11g.47448082C>ACA474430520RAPSNc.261G>T (p.Leu87=)
11g.47448082C>GCA474430519RAPSNc.261G>C (p.Leu87=)
11g.47448082C>TCA474430518RAPSNc.261G>A (p.Leu87=)
11g.47448083A=CA1969378574RAPSNc.260T= (p.Leu87=)
11g.47448083A>CCA380334862RAPSNc.260T>G (p.Leu87Arg)
11g.47448083A>GCA380334869RAPSNc.260T>C (p.Leu87Pro)
dbSNP gnomAD v2 gnomAD v4
11g.47448083A>TCA380334872RAPSNc.260T>A (p.Leu87Gln)
11g.47448084G>ACA5976772RAPSNc.259C>T (p.Leu87=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47448084G>CCA380334874RAPSNc.259C>G (p.Leu87Val)
gnomAD v4
11g.47448084G=CA1969378576RAPSNc.259C= (p.Leu87=)
11g.47448084G>TCA380334875RAPSNc.259C>A (p.Leu87Met)
11g.47448085G>ACA474430522RAPSNc.258C>T (p.Tyr86=)
ClinVar COSMIC
11g.47448085G>CCA380334876RAPSNc.258C>G (p.Tyr86Ter)
11g.47448085G>TCA380334877RAPSNc.258C>A (p.Tyr86Ter)
11g.47448086T>ACA380334881RAPSNc.257A>T (p.Tyr86Phe)
11g.47448086T>CCA380334883RAPSNc.257A>G (p.Tyr86Cys)
11g.47448086T>GCA380334887RAPSNc.257A>C (p.Tyr86Ser)
11g.47448087A=CA1969378583RAPSNc.256T= (p.Tyr86=)
11g.47448087A>CCA380334889RAPSNc.256T>G (p.Tyr86Asp)
11g.47448087A>GCA5976773RAPSNc.256T>C (p.Tyr86His)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47448087A>TCA380334898RAPSNc.256T>A (p.Tyr86Asn)
11g.47448088G>ACA474430524RAPSNc.255C>T (p.Ser85=)
11g.47448088G>CCA380334900RAPSNc.255C>G (p.Ser85Arg)
11g.47448088G>TCA380334904RAPSNc.255C>A (p.Ser85Arg)
11g.47448089C>ACA380334907RAPSNc.254G>T (p.Ser85Ile)
11g.47448089C=CA1969378588RAPSNc.254G= (p.Ser85=)
11g.47448089C>GCA380334909RAPSNc.254G>C (p.Ser85Thr)
dbSNP
11g.47448089C>TCA380334916RAPSNc.254G>A (p.Ser85Asn)
11g.47448090T>ACA380334920RAPSNc.253A>T (p.Ser85Cys)
11g.47448090T>CCA380334922RAPSNc.253A>G (p.Ser85Gly)
11g.47448090T>GCA380334933RAPSNc.253A>C (p.Ser85Arg)
11g.47448091C>ACA380334935RAPSNc.252G>T (p.Glu84Asp)
11g.47448091C>GCA380334937RAPSNc.252G>C (p.Glu84Asp)
11g.47448091C>TCA474430526RAPSNc.252G>A (p.Glu84=)
11g.47448092T>ACA380334939RAPSNc.251A>T (p.Glu84Val)
11g.47448092T>CCA380334941RAPSNc.251A>G (p.Glu84Gly)
11g.47448092T>GCA380334945RAPSNc.251A>C (p.Glu84Ala)
ClinVar dbSNP gnomAD v4
11g.47448093C>ACA380334957RAPSNc.250G>T (p.Glu84Ter)
11g.47448093C=CA1969378591RAPSNc.250G= (p.Glu84=)

Number of alleles fetched