Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.23538560_23538577delCA2576470471NPC1c.3008_3025del (p.Leu1003_Asn1008del)
c.2086_2103del
n.641_658del
n.351_368del
c.3059_3076del (p.Leu1020_Asn1025del)
c.2594_2611del (p.Leu865_Asn870del)
18g.23538561T>ACA401792116NPC1c.3022A>T (p.Asn1008Tyr)
c.2100A>T
n.655A>T
n.365A>T
c.3073A>T (p.Asn1025Tyr)
c.2608A>T (p.Asn870Tyr)
18g.23538561T>CCA401792117NPC1c.3022A>G (p.Asn1008Asp)
c.2100A>G
n.655A>G
n.365A>G
c.3073A>G (p.Asn1025Asp)
c.2608A>G (p.Asn870Asp)
18g.23538561T>GCA401792118NPC1c.3022A>C (p.Asn1008His)
c.2100A>C
n.655A>C
n.365A>C
c.3073A>C (p.Asn1025His)
c.2608A>C (p.Asn870His)
gnomAD v4
18g.23538562A>CCA503322455NPC1c.3021T>G (p.Pro1007=)
c.2099T>G
n.654T>G
n.364T>G
c.3072T>G (p.Pro1024=)
c.2607T>G (p.Pro869=)
18g.23538562A>GCA503322456NPC1c.3021T>C (p.Pro1007=)
c.2099T>C
n.654T>C
n.364T>C
c.3072T>C (p.Pro1024=)
c.2607T>C (p.Pro869=)
gnomAD v4
18g.23538562A>TCA503322457NPC1c.3021T>A (p.Pro1007=)
c.2099T>A
n.654T>A
n.364T>A
c.3072T>A (p.Pro1024=)
c.2607T>A (p.Pro869=)
18g.23538563G>ACA8912895NPC1c.3020C>T (p.Pro1007Leu)
c.2098C>T
n.653C>T
n.363C>T
c.3071C>T (p.Pro1024Leu)
c.2606C>T (p.Pro869Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.23538563G>CCA401792119NPC1c.3020C>G (p.Pro1007Arg)
c.2098C>G
n.653C>G
n.363C>G
c.3071C>G (p.Pro1024Arg)
c.2606C>G (p.Pro869Arg)
18g.23538563G=CA2290165351NPC1c.3020C= (p.Pro1007=)
c.2098C=
n.653C=
n.363C=
c.3071C= (p.Pro1024=)
c.2606C= (p.Pro869=)
18g.23538563G>TCA401792120NPC1c.3020C>A (p.Pro1007His)
c.2098C>A
n.653C>A
n.363C>A
c.3071C>A (p.Pro1024His)
c.2606C>A (p.Pro869His)
18g.23538564G>ACA401792121NPC1c.3019C>T (p.Pro1007Ser)
c.2097C>T
n.652C>T
n.362C>T
c.3070C>T (p.Pro1024Ser)
c.2605C>T (p.Pro869Ser)
18g.23538564G>CCA340032NPC1c.3019C>G (p.Pro1007Ala)
c.2097C>G
n.652C>G
n.362C>G
c.3070C>G (p.Pro1024Ala)
c.2605C>G (p.Pro869Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23538564G=CA2290165352NPC1c.3019C= (p.Pro1007=)
c.2097C=
n.652C=
n.362C=
c.3070C= (p.Pro1024=)
c.2605C= (p.Pro869=)
18g.23538564G>TCA401792122NPC1c.3019C>A (p.Pro1007Thr)
c.2097C>A
n.652C>A
n.362C>A
c.3070C>A (p.Pro1024Thr)
c.2605C>A (p.Pro869Thr)
18g.23538565G>ACA503322458NPC1c.3018C>T (p.Asn1006=)
c.2096C>T
n.651C>T
n.361C>T
c.3069C>T (p.Asn1023=)
c.2604C>T (p.Asn868=)
18g.23538565G>CCA401792123NPC1c.3018C>G (p.Asn1006Lys)
c.2096C>G
n.651C>G
n.361C>G
c.3069C>G (p.Asn1023Lys)
c.2604C>G (p.Asn868Lys)
18g.23538565G>TCA401792124NPC1c.3018C>A (p.Asn1006Lys)
c.2096C>A
n.651C>A
n.361C>A
c.3069C>A (p.Asn1023Lys)
c.2604C>A (p.Asn868Lys)
18g.23538566T>ACA401792126NPC1c.3017A>T (p.Asn1006Ile)
c.2095A>T
n.650A>T
n.360A>T
c.3068A>T (p.Asn1023Ile)
c.2603A>T (p.Asn868Ile)
gnomAD v4
18g.23538566T>CCA401792127NPC1c.3017A>G (p.Asn1006Ser)
c.2095A>G
n.650A>G
n.360A>G
c.3068A>G (p.Asn1023Ser)
c.2603A>G (p.Asn868Ser)
18g.23538566T>GCA401792125NPC1c.3017A>C (p.Asn1006Thr)
c.2095A>C
n.650A>C
n.360A>C
c.3068A>C (p.Asn1023Thr)
c.2603A>C (p.Asn868Thr)
dbSNP
18g.23538566T=CA2290165353NPC1c.3017A= (p.Asn1006=)
c.2095A=
n.650A=
n.360A=
c.3068A= (p.Asn1023=)
c.2603A= (p.Asn868=)
18g.23538567delCA2580095497NPC1c.3017del (p.Asn1006ThrfsTer?)
c.2095del
n.650del
n.360del
c.3068del (p.Asn1023ThrfsTer?)
c.2603del (p.Asn868ThrfsTer?)
ClinVar
18g.23538567T>ACA401792128NPC1c.3016A>T (p.Asn1006Tyr)
c.2094A>T
n.649A>T
n.359A>T
c.3067A>T (p.Asn1023Tyr)
c.2602A>T (p.Asn868Tyr)
18g.23538567T>CCA401792130NPC1c.3016A>G (p.Asn1006Asp)
c.2094A>G
n.649A>G
n.359A>G
c.3067A>G (p.Asn1023Asp)
c.2602A>G (p.Asn868Asp)
gnomAD v4
18g.23538567T>GCA401792129NPC1c.3016A>C (p.Asn1006His)
c.2094A>C
n.649A>C
n.359A>C
c.3067A>C (p.Asn1023His)
c.2602A>C (p.Asn868His)
18g.23538568A>CCA401792131NPC1c.3015T>G (p.Asp1005Glu)
c.2093T>G
n.648T>G
n.358T>G
c.3066T>G (p.Asp1022Glu)
c.2601T>G (p.Asp867Glu)
18g.23538568A>GCA503322459NPC1c.3015T>C (p.Asp1005=)
c.2093T>C
n.648T>C
n.358T>C
c.3066T>C (p.Asp1022=)
c.2601T>C (p.Asp867=)
18g.23538568A>TCA401792132NPC1c.3015T>A (p.Asp1005Glu)
c.2093T>A
n.648T>A
n.358T>A
c.3066T>A (p.Asp1022Glu)
c.2601T>A (p.Asp867Glu)
18g.23538569T>ACA401792133NPC1c.3014A>T (p.Asp1005Val)
c.2092A>T
n.647A>T
n.357A>T
c.3065A>T (p.Asp1022Val)
c.2600A>T (p.Asp867Val)
18g.23538569T>CCA401792134NPC1c.3014A>G (p.Asp1005Gly)
c.2092A>G
n.647A>G
n.357A>G
c.3065A>G (p.Asp1022Gly)
c.2600A>G (p.Asp867Gly)
18g.23538569T>GCA401792135NPC1c.3014A>C (p.Asp1005Ala)
c.2092A>C
n.647A>C
n.357A>C
c.3065A>C (p.Asp1022Ala)
c.2600A>C (p.Asp867Ala)
18g.23538570C>ACA401792136NPC1c.3013G>T (p.Asp1005Tyr)
c.2091G>T
n.646G>T
n.356G>T
c.3064G>T (p.Asp1022Tyr)
c.2599G>T (p.Asp867Tyr)
18g.23538570C>GCA401792137NPC1c.3013G>C (p.Asp1005His)
c.2091G>C
n.646G>C
n.356G>C
c.3064G>C (p.Asp1022His)
c.2599G>C (p.Asp867His)
18g.23538570C>TCA401792138NPC1c.3013G>A (p.Asp1005Asn)
c.2091G>A
n.646G>A
n.356G>A
c.3064G>A (p.Asp1022Asn)
c.2599G>A (p.Asp867Asn)
18g.23538571C>ACA503322460NPC1c.3012G>T (p.Ser1004=)
c.2090G>T
n.645G>T
n.355G>T
c.3063G>T (p.Ser1021=)
c.2598G>T (p.Ser866=)
18g.23538571C=CA2290165354NPC1c.3012G= (p.Ser1004=)
c.2090G=
n.645G=
n.355G=
c.3063G= (p.Ser1021=)
c.2598G= (p.Ser866=)
18g.23538571C>GCA503322461NPC1c.3012G>C (p.Ser1004=)
c.2090G>C
n.645G>C
n.355G>C
c.3063G>C (p.Ser1021=)
c.2598G>C (p.Ser866=)
ClinVar dbSNP gnomAD v3 gnomAD v4
18g.23538571C>TCA8912896NPC1c.3012G>A (p.Ser1004=)
c.2090G>A
n.645G>A
n.355G>A
c.3063G>A (p.Ser1021=)
c.2598G>A (p.Ser866=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23538572G>ACA8912897NPC1c.3011C>T (p.Ser1004Leu)
c.2089C>T
n.644C>T
n.354C>T
c.3062C>T (p.Ser1021Leu)
c.2597C>T (p.Ser866Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23538572G>CCA401792140NPC1c.3011C>G (p.Ser1004Trp)
c.2089C>G
n.644C>G
n.354C>G
c.3062C>G (p.Ser1021Trp)
c.2597C>G (p.Ser866Trp)
18g.23538572G=CA2290165355NPC1c.3011C= (p.Ser1004=)
c.2089C=
n.644C=
n.354C=
c.3062C= (p.Ser1021=)
c.2597C= (p.Ser866=)
18g.23538572G>TCA401792139NPC1c.3011C>A (p.Ser1004Ter)
c.2089C>A
n.644C>A
n.354C>A
c.3062C>A (p.Ser1021Ter)
c.2597C>A (p.Ser866Ter)
18g.23538573A>CCA401792141NPC1c.3010T>G (p.Ser1004Ala)
c.2088T>G
n.643T>G
n.353T>G
c.3061T>G (p.Ser1021Ala)
c.2596T>G (p.Ser866Ala)
18g.23538573A>GCA401792142NPC1c.3010T>C (p.Ser1004Pro)
c.2088T>C
n.643T>C
n.353T>C
c.3061T>C (p.Ser1021Pro)
c.2596T>C (p.Ser866Pro)
18g.23538573A>TCA401792143NPC1c.3010T>A (p.Ser1004Thr)
c.2088T>A
n.643T>A
n.353T>A
c.3061T>A (p.Ser1021Thr)
c.2596T>A (p.Ser866Thr)
18g.23538574A>CCA503322462NPC1c.3009T>G (p.Leu1003=)
c.2087T>G
n.642T>G
n.352T>G
c.3060T>G (p.Leu1020=)
c.2595T>G (p.Leu865=)
18g.23538574A>GCA503322463NPC1c.3009T>C (p.Leu1003=)
c.2087T>C
n.642T>C
n.352T>C
c.3060T>C (p.Leu1020=)
c.2595T>C (p.Leu865=)
18g.23538574A>TCA503322464NPC1c.3009T>A (p.Leu1003=)
c.2087T>A
n.642T>A
n.352T>A
c.3060T>A (p.Leu1020=)
c.2595T>A (p.Leu865=)
18g.23538575A>CCA401792144NPC1c.3008T>G (p.Leu1003Arg)
c.2086T>G
n.641T>G
n.351T>G
c.3059T>G (p.Leu1020Arg)
c.2594T>G (p.Leu865Arg)

Number of alleles fetched