Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.71444036G>ACA221665DHCR7c.278C>T (p.Thr93Met)
c.104C>T (p.Thr35Met)
n.555C>T
c.-308C>T (n.-308C>T)
c.182C>T (p.Thr61Met)
c.218C>T (p.Thr73Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.71444036G>CCA381696166DHCR7c.278C>G (p.Thr93Arg)
c.104C>G (p.Thr35Arg)
n.555C>G
c.-308C>G (n.-308C>G)
c.182C>G (p.Thr61Arg)
c.218C>G (p.Thr73Arg)
11g.71444036G=CA1981491030DHCR7c.278C= (p.Thr93=)
c.104C= (p.Thr35=)
n.555C=
c.-308C= (n.-308C=)
c.182C= (p.Thr61=)
c.218C= (p.Thr73=)
11g.71444036G>TCA381696172DHCR7c.278C>A (p.Thr93Lys)
c.104C>A (p.Thr35Lys)
n.555C>A
c.-308C>A (n.-308C>A)
c.182C>A (p.Thr61Lys)
c.218C>A (p.Thr73Lys)
ClinVar
11g.71444037T>ACA381696176DHCR7c.277A>T (p.Thr93Ser)
c.103A>T (p.Thr35Ser)
n.554A>T
c.-309A>T (n.-309A>T)
c.181A>T (p.Thr61Ser)
c.217A>T (p.Thr73Ser)
11g.71444037T>CCA381696179DHCR7c.277A>G (p.Thr93Ala)
c.103A>G (p.Thr35Ala)
n.554A>G
c.-309A>G (n.-309A>G)
c.181A>G (p.Thr61Ala)
c.217A>G (p.Thr73Ala)
11g.71444037T>GCA381696182DHCR7c.277A>C (p.Thr93Pro)
c.103A>C (p.Thr35Pro)
n.554A>C
c.-309A>C (n.-309A>C)
c.181A>C (p.Thr61Pro)
c.217A>C (p.Thr73Pro)
11g.71444038T>ACA475520222DHCR7c.276A>T (p.Ile92=)
c.102A>T (p.Ile34=)
n.553A>T
c.-310A>T (n.-310A>T)
c.180A>T (p.Ile60=)
c.216A>T (p.Ile72=)
11g.71444038T>CCA381696196DHCR7c.276A>G (p.Ile92Met)
c.102A>G (p.Ile34Met)
n.553A>G
c.-310A>G (n.-310A>G)
c.180A>G (p.Ile60Met)
c.216A>G (p.Ile72Met)
11g.71444038T>GCA475520225DHCR7c.276A>C (p.Ile92=)
c.102A>C (p.Ile34=)
n.553A>C
c.-310A>C (n.-310A>C)
c.180A>C (p.Ile60=)
c.216A>C (p.Ile72=)
11g.71444039A>CCA381696198DHCR7c.275T>G (p.Ile92Arg)
c.101T>G (p.Ile34Arg)
n.552T>G
c.-311T>G (n.-311T>G)
c.179T>G (p.Ile60Arg)
c.215T>G (p.Ile72Arg)
11g.71444039A>GCA381696201DHCR7c.275T>C (p.Ile92Thr)
c.101T>C (p.Ile34Thr)
n.552T>C
c.-311T>C (n.-311T>C)
c.179T>C (p.Ile60Thr)
c.215T>C (p.Ile72Thr)
11g.71444039A>TCA381696204DHCR7c.275T>A (p.Ile92Lys)
c.101T>A (p.Ile34Lys)
n.552T>A
c.-311T>A (n.-311T>A)
c.179T>A (p.Ile60Lys)
c.215T>A (p.Ile72Lys)
gnomAD v4
11g.71444040T>ACA381696207DHCR7c.274A>T (p.Ile92Leu)
c.100A>T (p.Ile34Leu)
n.551A>T
c.-312A>T (n.-312A>T)
c.178A>T (p.Ile60Leu)
c.214A>T (p.Ile72Leu)
11g.71444040T>CCA381696211DHCR7c.274A>G (p.Ile92Val)
c.100A>G (p.Ile34Val)
n.551A>G
c.-312A>G (n.-312A>G)
c.178A>G (p.Ile60Val)
c.214A>G (p.Ile72Val)
gnomAD v4
11g.71444040T>GCA381696209DHCR7c.274A>C (p.Ile92Leu)
c.100A>C (p.Ile34Leu)
n.551A>C
c.-312A>C (n.-312A>C)
c.178A>C (p.Ile60Leu)
c.214A>C (p.Ile72Leu)
11g.71444041A=CA1981491031DHCR7c.273T= (p.Pro91=)
c.99T= (p.Pro33=)
n.550T=
c.-313T= (n.-313T=)
c.177T= (p.Pro59=)
c.213T= (p.Pro71=)
11g.71444041A>CCA475520240DHCR7c.273T>G (p.Pro91=)
c.99T>G (p.Pro33=)
n.550T>G
c.-313T>G (n.-313T>G)
c.177T>G (p.Pro59=)
c.213T>G (p.Pro71=)
11g.71444041A>GCA6162648DHCR7c.273T>C (p.Pro91=)
c.99T>C (p.Pro33=)
n.550T>C
c.-313T>C (n.-313T>C)
c.177T>C (p.Pro59=)
c.213T>C (p.Pro71=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.71444041A>TCA475520242DHCR7c.273T>A (p.Pro91=)
c.99T>A (p.Pro33=)
n.550T>A
c.-313T>A (n.-313T>A)
c.177T>A (p.Pro59=)
c.213T>A (p.Pro71=)
ClinVar dbSNP
11g.71444042G>ACA381696213DHCR7c.272C>T (p.Pro91Leu)
c.98C>T (p.Pro33Leu)
n.549C>T
c.-314C>T (n.-314C>T)
c.176C>T (p.Pro59Leu)
c.212C>T (p.Pro71Leu)
dbSNP gnomAD v2 gnomAD v4
11g.71444042G>CCA381696215DHCR7c.272C>G (p.Pro91Arg)
c.98C>G (p.Pro33Arg)
n.549C>G
c.-314C>G (n.-314C>G)
c.176C>G (p.Pro59Arg)
c.212C>G (p.Pro71Arg)
11g.71444042G=CA1981491032DHCR7c.272C= (p.Pro91=)
c.98C= (p.Pro33=)
n.549C=
c.-314C= (n.-314C=)
c.176C= (p.Pro59=)
c.212C= (p.Pro71=)
11g.71444042G>TCA381696216DHCR7c.272C>A (p.Pro91His)
c.98C>A (p.Pro33His)
n.549C>A
c.-314C>A (n.-314C>A)
c.176C>A (p.Pro59His)
c.212C>A (p.Pro71His)
11g.71444043G>ACA381696218DHCR7c.271C>T (p.Pro91Ser)
c.97C>T (p.Pro33Ser)
n.548C>T
c.-315C>T (n.-315C>T)
c.175C>T (p.Pro59Ser)
c.211C>T (p.Pro71Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.71444043G>CCA381696221DHCR7c.271C>G (p.Pro91Ala)
c.97C>G (p.Pro33Ala)
n.548C>G
c.-315C>G (n.-315C>G)
c.175C>G (p.Pro59Ala)
c.211C>G (p.Pro71Ala)
11g.71444043G=CA1981491033DHCR7c.271C= (p.Pro91=)
c.97C= (p.Pro33=)
n.548C=
c.-315C= (n.-315C=)
c.175C= (p.Pro59=)
c.211C= (p.Pro71=)
11g.71444043G>TCA381696220DHCR7c.271C>A (p.Pro91Thr)
c.97C>A (p.Pro33Thr)
n.548C>A
c.-315C>A (n.-315C>A)
c.175C>A (p.Pro59Thr)
c.211C>A (p.Pro71Thr)
11g.71444044T>ACA475520258DHCR7c.270A>T (p.Pro90=)
c.96A>T (p.Pro32=)
n.547A>T
c.-316A>T (n.-316A>T)
c.174A>T (p.Pro58=)
c.210A>T (p.Pro70=)
11g.71444044T>CCA475520261DHCR7c.270A>G (p.Pro90=)
c.96A>G (p.Pro32=)
n.547A>G
c.-316A>G (n.-316A>G)
c.174A>G (p.Pro58=)
c.210A>G (p.Pro70=)
ClinVar dbSNP
11g.71444044T>GCA475520264DHCR7c.270A>C (p.Pro90=)
c.96A>C (p.Pro32=)
n.547A>C
c.-316A>C (n.-316A>C)
c.174A>C (p.Pro58=)
c.210A>C (p.Pro70=)
11g.71444044T=CA1981491034DHCR7c.270A= (p.Pro90=)
c.96A= (p.Pro32=)
n.547A=
c.-316A= (n.-316A=)
c.174A= (p.Pro58=)
c.210A= (p.Pro70=)
11g.71444045G>ACA381696223DHCR7c.269C>T (p.Pro90Leu)
c.95C>T (p.Pro32Leu)
n.546C>T
c.-317C>T (n.-317C>T)
c.173C>T (p.Pro58Leu)
c.209C>T (p.Pro70Leu)
11g.71444045G>CCA381696225DHCR7c.269C>G (p.Pro90Arg)
c.95C>G (p.Pro32Arg)
n.546C>G
c.-317C>G (n.-317C>G)
c.173C>G (p.Pro58Arg)
c.209C>G (p.Pro70Arg)
11g.71444045G>TCA381696227DHCR7c.269C>A (p.Pro90Gln)
c.95C>A (p.Pro32Gln)
n.546C>A
c.-317C>A (n.-317C>A)
c.173C>A (p.Pro58Gln)
c.209C>A (p.Pro70Gln)
11g.71444046G>ACA6162649DHCR7c.268C>T (p.Pro90Ser)
c.94C>T (p.Pro32Ser)
n.545C>T
c.-318C>T (n.-318C>T)
c.172C>T (p.Pro58Ser)
c.208C>T (p.Pro70Ser)
dbSNP ExAC gnomAD v2
11g.71444046G>CCA381696230DHCR7c.268C>G (p.Pro90Ala)
c.94C>G (p.Pro32Ala)
n.545C>G
c.-318C>G (n.-318C>G)
c.172C>G (p.Pro58Ala)
c.208C>G (p.Pro70Ala)
11g.71444046G=CA1981491035DHCR7c.268C= (p.Pro90=)
c.94C= (p.Pro32=)
n.545C=
c.-318C= (n.-318C=)
c.172C= (p.Pro58=)
c.208C= (p.Pro70=)
11g.71444046G>TCA381696234DHCR7c.268C>A (p.Pro90Thr)
c.94C>A (p.Pro32Thr)
n.545C>A
c.-318C>A (n.-318C>A)
c.172C>A (p.Pro58Thr)
c.208C>A (p.Pro70Thr)
11g.71444047A=CA1981491036DHCR7c.267T= (p.Thr89=)
c.93T= (p.Thr31=)
n.544T=
c.-319T= (n.-319T=)
c.171T= (p.Thr57=)
c.207T= (p.Thr69=)
11g.71444047A>CCA475520277DHCR7c.267T>G (p.Thr89=)
c.93T>G (p.Thr31=)
n.544T>G
c.-319T>G (n.-319T>G)
c.171T>G (p.Thr57=)
c.207T>G (p.Thr69=)
gnomAD v4
11g.71444047A>GCA6162650DHCR7c.267T>C (p.Thr89=)
c.93T>C (p.Thr31=)
n.544T>C
c.-319T>C (n.-319T>C)
c.171T>C (p.Thr57=)
c.207T>C (p.Thr69=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.71444047A>TCA475520280DHCR7c.267T>A (p.Thr89=)
c.93T>A (p.Thr31=)
n.544T>A
c.-319T>A (n.-319T>A)
c.171T>A (p.Thr57=)
c.207T>A (p.Thr69=)
dbSNP
11g.71444048delCA2697548793DHCR7c.266del (p.Thr89IlefsTer4)
c.92del (p.Thr31IlefsTer4)
n.543del
c.-320del (n.-320del)
c.170del (p.Thr57IlefsTer4)
c.266del (p.Thr89IlefsTer?)
c.206del (p.Thr69IlefsTer4)
ClinVar
11g.71444048G>ACA381696237DHCR7c.266C>T (p.Thr89Ile)
c.92C>T (p.Thr31Ile)
n.543C>T
c.-320C>T (n.-320C>T)
c.170C>T (p.Thr57Ile)
c.206C>T (p.Thr69Ile)
11g.71444048G>CCA381696238DHCR7c.266C>G (p.Thr89Ser)
c.92C>G (p.Thr31Ser)
n.543C>G
c.-320C>G (n.-320C>G)
c.170C>G (p.Thr57Ser)
c.206C>G (p.Thr69Ser)
dbSNP gnomAD v3 gnomAD v4
11g.71444048G=CA1981491037DHCR7c.266C= (p.Thr89=)
c.92C= (p.Thr31=)
n.543C=
c.-320C= (n.-320C=)
c.170C= (p.Thr57=)
c.206C= (p.Thr69=)
11g.71444048G>TCA381696240DHCR7c.266C>A (p.Thr89Asn)
c.92C>A (p.Thr31Asn)
n.543C>A
c.-320C>A (n.-320C>A)
c.170C>A (p.Thr57Asn)
c.206C>A (p.Thr69Asn)
11g.71444049T>ACA224280811DHCR7c.265A>T (p.Thr89Ser)
c.91A>T (p.Thr31Ser)
n.542A>T
c.-321A>T (n.-321A>T)
c.169A>T (p.Thr57Ser)
c.205A>T (p.Thr69Ser)
dbSNP
11g.71444049T>CCA224280813DHCR7c.265A>G (p.Thr89Ala)
c.91A>G (p.Thr31Ala)
n.542A>G
c.-321A>G (n.-321A>G)
c.169A>G (p.Thr57Ala)
c.205A>G (p.Thr69Ala)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched