Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.131851230G>ACA452154635ENPP1c.519G>A (p.Lys173=)
c.197G>A
c.108+1124G>A
n.539G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.131851230G>CCA365662023ENPP1c.519G>C (p.Lys173Asn)
c.197G>C
c.108+1124G>C
n.539G>C
6g.131851230G=CA1664253754ENPP1c.519G= (p.Lys173=)
c.197G=
c.108+1124G=
n.539G=
6g.131851230G>TCA365662025ENPP1c.519G>T (p.Lys173Asn)
c.197G>T
c.108+1124G>T
n.539G>T
6g.131851231G>ACA365662028ENPP1c.520G>A (p.Gly174Ser)
c.198G>A
c.108+1125G>A
n.540G>A
dbSNP gnomAD v3 gnomAD v4
6g.131851231G>CCA365662031ENPP1c.520G>C (p.Gly174Arg)
c.198G>C
c.108+1125G>C
n.540G>C
6g.131851231G=CA1664253755ENPP1c.520G= (p.Gly174=)
c.198G=
c.108+1125G=
n.540G=
6g.131851231G>TCA365662037ENPP1c.520G>T (p.Gly174Cys)
c.198G>T
c.108+1125G>T
n.540G>T
6g.131851232G>ACA365662043ENPP1c.521G>A (p.Gly174Asp)
c.199G>A
c.108+1126G>A
n.541G>A
6g.131851232G>CCA365662048ENPP1c.521G>C (p.Gly174Ala)
c.199G>C
c.108+1126G>C
n.541G>C
6g.131851232G>TCA365662051ENPP1c.521G>T (p.Gly174Val)
c.199G>T
c.108+1126G>T
n.541G>T
6g.131851233C>ACA452154637ENPP1c.522C>A (p.Gly174=)
c.200C>A
c.108+1127C>A
n.542C>A
6g.131851233C=CA1664253756ENPP1c.522C= (p.Gly174=)
c.200C=
c.108+1127C=
n.542C=
6g.131851233C>GCA4001919ENPP1c.522C>G (p.Gly174=)
c.200C>G
c.108+1127C>G
n.542C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.131851233C>TCA4001918ENPP1c.522C>T (p.Gly174=)
c.200C>T
c.108+1127C>T
n.542C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.131851234delCA2773093457ENPP1c.523del (p.Asp175ThrfsTer17)
c.201del
c.108+1128del
n.543del
6g.131851234G>ACA4001920ENPP1c.523G>A (p.Asp175Asn)
c.201G>A
c.108+1128G>A
n.543G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.131851234G>CCA365662069ENPP1c.523G>C (p.Asp175His)
c.201G>C
c.108+1128G>C
n.543G>C
6g.131851234G=CA1664253757ENPP1c.523G= (p.Asp175=)
c.201G=
c.108+1128G=
n.543G=
6g.131851234G>TCA365662073ENPP1c.523G>T (p.Asp175Tyr)
c.201G>T
c.108+1128G>T
n.543G>T
gnomAD v4
6g.131851235A>CCA365662102ENPP1c.524A>C (p.Asp175Ala)
c.202A>C
c.108+1129A>C
n.544A>C
6g.131851235A>GCA365662106ENPP1c.524A>G (p.Asp175Gly)
c.202A>G
c.108+1129A>G
n.544A>G
6g.131851235A>TCA365662098ENPP1c.524A>T (p.Asp175Val)
c.202A>T
c.108+1129A>T
n.544A>T
6g.131851236C>ACA365662109ENPP1c.525C>A (p.Asp175Glu)
c.203C>A
c.108+1130C>A
n.545C>A
6g.131851236C=CA1664253758ENPP1c.525C= (p.Asp175=)
c.203C=
c.108+1130C=
n.545C=
6g.131851236C>GCA365662110ENPP1c.525C>G (p.Asp175Glu)
c.203C>G
c.108+1130C>G
n.545C>G
6g.131851236C>TCA4001921ENPP1c.525C>T (p.Asp175=)
c.203C>T
c.108+1130C>T
n.545C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.131851237T>ACA365662112ENPP1c.526T>A (p.Cys176Ser)
c.204T>A
c.108+1131T>A
n.546T>A
6g.131851237T>CCA365662115ENPP1c.526T>C (p.Cys176Arg)
c.204T>C
c.108+1131T>C
n.546T>C
6g.131851237T>GCA365662118ENPP1c.526T>G (p.Cys176Gly)
c.204T>G
c.108+1131T>G
n.546T>G
6g.131851238G>ACA365662123ENPP1c.527G>A (p.Cys176Tyr)
c.205G>A
c.108+1132G>A
n.547G>A
gnomAD v4
6g.131851238G>CCA365662129ENPP1c.527G>C (p.Cys176Ser)
c.205G>C
c.108+1132G>C
n.547G>C
6g.131851238G>TCA365662131ENPP1c.527G>T (p.Cys176Phe)
c.205G>T
c.108+1132G>T
n.547G>T
6g.131851239C>ACA365662136ENPP1c.528C>A (p.Cys176Ter)
c.206C>A
c.108+1133C>A
n.548C>A
6g.131851239C>GCA365662141ENPP1c.528C>G (p.Cys176Trp)
c.206C>G
c.108+1133C>G
n.548C>G
6g.131851239C>TCA452154646ENPP1c.528C>T (p.Cys176=)
c.206C>T
c.108+1133C>T
n.548C>T
COSMIC COSMIC
6g.131851240T>ACA365662154ENPP1c.529T>A (p.Cys177Ser)
c.207T>A
c.108+1134T>A
n.549T>A
6g.131851240T>CCA365662149ENPP1c.529T>C (p.Cys177Arg)
c.207T>C
c.108+1134T>C
n.549T>C
6g.131851240T>GCA365662146ENPP1c.529T>G (p.Cys177Gly)
c.207T>G
c.108+1134T>G
n.549T>G
6g.131851241G>ACA145330ENPP1c.530G>A (p.Cys177Tyr)
c.208G>A
c.108+1135G>A
n.550G>A
ClinVar dbSNP
6g.131851241G>CCA365662183ENPP1c.530G>C (p.Cys177Ser)
c.208G>C
c.108+1135G>C
n.550G>C
6g.131851241G=CA1664253759ENPP1c.530G= (p.Cys177=)
c.208G=
c.108+1135G=
n.550G=
6g.131851241G>TCA365662186ENPP1c.530G>T (p.Cys177Phe)
c.208G>T
c.108+1135G>T
n.550G>T
6g.131851242C>ACA365662194ENPP1c.531C>A (p.Cys177Ter)
c.209C>A
c.108+1136C>A
n.551C>A
6g.131851242C=CA1664253760ENPP1c.531C= (p.Cys177=)
c.209C=
c.108+1136C=
n.551C=
6g.131851242C>GCA365662201ENPP1c.531C>G (p.Cys177Trp)
c.209C>G
c.108+1136C>G
n.551C>G
gnomAD v4
6g.131851242C>TCA4001922ENPP1c.531C>T (p.Cys177=)
c.209C>T
c.108+1136C>T
n.551C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.131851243A=CA1664253761ENPP1c.532A= (p.Ile178=)
c.210A=
c.108+1137A=
n.552A=
6g.131851243A>CCA365662210ENPP1c.532A>C (p.Ile178Leu)
c.210A>C
c.108+1137A>C
n.552A>C
6g.131851243A>GCA147926407ENPP1c.532A>G (p.Ile178Val)
c.210A>G
c.108+1137A>G
n.552A>G
dbSNP gnomAD v4

Number of alleles fetched