Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.23561370A>CCA503325327NPC1c.621T>G (p.Pro207=)
n.535T>G
c.156T>G (p.Pro52=)
18g.23561370A>GCA503325328NPC1c.621T>C (p.Pro207=)
n.535T>C
c.156T>C (p.Pro52=)
18g.23561370A>TCA503325329NPC1c.621T>A (p.Pro207=)
n.535T>A
c.156T>A (p.Pro52=)
18g.23561371G>ACA401782074NPC1c.620C>T (p.Pro207Leu)
n.534C>T
c.155C>T (p.Pro52Leu)
ClinVar dbSNP gnomAD v4 COSMIC
18g.23561371G>CCA401782076NPC1c.620C>G (p.Pro207Arg)
n.534C>G
c.155C>G (p.Pro52Arg)
18g.23561371G=CA2290176158NPC1c.620C= (p.Pro207=)
n.534C=
c.155C= (p.Pro52=)
18g.23561371G>TCA401782077NPC1c.620C>A (p.Pro207His)
n.534C>A
c.155C>A (p.Pro52His)
18g.23561371_23561375delinsGGAGTCA2290176157NPC1c.616_620delinsACTCC (p.Thr206=)
n.530_534delinsACTCC
c.151_155delinsACTCC (p.Thr51=)
18g.23561372G>ACA401782078NPC1c.619C>T (p.Pro207Ser)
n.533C>T
c.154C>T (p.Pro52Ser)
ClinVar gnomAD v4 COSMIC
18g.23561372G>CCA401782081NPC1c.619C>G (p.Pro207Ala)
n.533C>G
c.154C>G (p.Pro52Ala)
18g.23561372G>TCA401782083NPC1c.619C>A (p.Pro207Thr)
n.533C>A
c.154C>A (p.Pro52Thr)
18g.23561374_23561377delCA628978914NPC1c.616_619del (p.Thr206LeufsTer14)
n.530_533del
c.151_154del (p.Thr51LeufsTer14)
dbSNP gnomAD v2 gnomAD v4
18g.23561373A>CCA503325330NPC1c.618T>G (p.Thr206=)
n.532T>G
c.153T>G (p.Thr51=)
18g.23561373A>GCA503325331NPC1c.618T>C (p.Thr206=)
n.532T>C
c.153T>C (p.Thr51=)
18g.23561373A>TCA503325332NPC1c.618T>A (p.Thr206=)
n.532T>A
c.153T>A (p.Thr51=)
18g.23561374G>ACA401782092NPC1c.617C>T (p.Thr206Ile)
n.531C>T
c.152C>T (p.Thr51Ile)
dbSNP gnomAD v2 gnomAD v4 COSMIC
18g.23561374G>CCA401782086NPC1c.617C>G (p.Thr206Ser)
n.531C>G
c.152C>G (p.Thr51Ser)
18g.23561374G=CA2290176159NPC1c.617C= (p.Thr206=)
n.531C=
c.152C= (p.Thr51=)
18g.23561374G>TCA401782089NPC1c.617C>A (p.Thr206Asn)
n.531C>A
c.152C>A (p.Thr51Asn)
18g.23561375T>ACA8913696NPC1c.616A>T (p.Thr206Ser)
n.530A>T
c.151A>T (p.Thr51Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
18g.23561375T>CCA401782093NPC1c.616A>G (p.Thr206Ala)
n.530A>G
c.151A>G (p.Thr51Ala)
18g.23561375T>GCA401782094NPC1c.616A>C (p.Thr206Pro)
n.530A>C
c.151A>C (p.Thr51Pro)
18g.23561375T=CA2290176160NPC1c.616A= (p.Thr206=)
n.530A=
c.151A= (p.Thr51=)
18g.23561376G>ACA8913697NPC1c.615C>T (p.Ile205=)
n.529C>T
c.150C>T (p.Ile50=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.23561376G>CCA401782097NPC1c.615C>G (p.Ile205Met)
n.529C>G
c.150C>G (p.Ile50Met)
18g.23561376G=CA2290176161NPC1c.615C= (p.Ile205=)
n.529C=
c.150C= (p.Ile50=)
18g.23561376G>TCA503325333NPC1c.615C>A (p.Ile205=)
n.529C>A
c.150C>A (p.Ile50=)
18g.23561377A>CCA401782098NPC1c.614T>G (p.Ile205Ser)
n.528T>G
c.149T>G (p.Ile50Ser)
18g.23561377A>GCA401782099NPC1c.614T>C (p.Ile205Thr)
n.528T>C
c.149T>C (p.Ile50Thr)
18g.23561377A>TCA401782100NPC1c.614T>A (p.Ile205Asn)
n.528T>A
c.149T>A (p.Ile50Asn)
18g.23561378T>ACA401782102NPC1c.613A>T (p.Ile205Phe)
n.527A>T
c.148A>T (p.Ile50Phe)
18g.23561378T>CCA8913698NPC1c.613A>G (p.Ile205Val)
n.527A>G
c.148A>G (p.Ile50Val)
dbSNP ExAC gnomAD v2 gnomAD v4
18g.23561378T>GCA401782104NPC1c.613A>C (p.Ile205Leu)
n.527A>C
c.148A>C (p.Ile50Leu)
18g.23561378T=CA2290176162NPC1c.613A= (p.Ile205=)
n.527A=
c.148A= (p.Ile50=)
18g.23561378_23561379delinsTGCA2290176163NPC1c.612_613delinsCA (p.Thr204=)
n.526_527delinsCA
c.147_148delinsCA (p.Thr49=)
18g.23561379G>ACA202999NPC1c.612C>T (p.Thr204=)
n.526C>T
c.147C>T (p.Thr49=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23561379G>CCA503325335NPC1c.612C>G (p.Thr204=)
n.526C>G
c.147C>G (p.Thr49=)
18g.23561379G=CA2290176165NPC1c.612C= (p.Thr204=)
n.526C=
c.147C= (p.Thr49=)
18g.23561379G>TCA503325334NPC1c.612C>A (p.Thr204=)
n.526C>A
c.147C>A (p.Thr49=)
dbSNP
18g.23561380delCA2290176164NPC1c.612del (p.Ile205SerfsTer16)
n.526del
c.147del (p.Ile50SerfsTer16)
18g.23561380G>ACA401782109NPC1c.611C>T (p.Thr204Ile)
n.525C>T
c.146C>T (p.Thr49Ile)
18g.23561380G>CCA401782111NPC1c.611C>G (p.Thr204Ser)
n.525C>G
c.146C>G (p.Thr49Ser)
18g.23561380G>TCA401782107NPC1c.611C>A (p.Thr204Asn)
n.525C>A
c.146C>A (p.Thr49Asn)
18g.23561381T>ACA401782112NPC1c.610A>T (p.Thr204Ser)
n.524A>T
c.145A>T (p.Thr49Ser)
18g.23561381T>CCA401782114NPC1c.610A>G (p.Thr204Ala)
n.524A>G
c.145A>G (p.Thr49Ala)
ClinVar dbSNP gnomAD v4
18g.23561381T>GCA401782113NPC1c.610A>C (p.Thr204Pro)
n.524A>C
c.145A>C (p.Thr49Pro)
18g.23561381T=CA2290176166NPC1c.610A= (p.Thr204=)
n.524A=
c.145A= (p.Thr49=)
18g.23561382A>CCA401782115NPC1c.609T>G (p.Phe203Leu)
n.523T>G
c.144T>G (p.Phe48Leu)
18g.23561382A>GCA503325336NPC1c.609T>C (p.Phe203=)
n.523T>C
c.144T>C (p.Phe48=)
18g.23561382A>TCA401782116NPC1c.609T>A (p.Phe203Leu)
n.523T>A
c.144T>A (p.Phe48Leu)
gnomAD v4

Number of alleles fetched