Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.23538560_23538577del | CA2576470471 | NPC1 | c.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) | |
18 | g.23538561T>A | CA401792116 | NPC1 | c.3022A>T (p.Asn1008Tyr) c.2100A>T n.655A>T n.365A>T c.3073A>T (p.Asn1025Tyr) c.2608A>T (p.Asn870Tyr) | |
18 | g.23538561T>C | CA401792117 | NPC1 | c.3022A>G (p.Asn1008Asp) c.2100A>G n.655A>G n.365A>G c.3073A>G (p.Asn1025Asp) c.2608A>G (p.Asn870Asp) | |
18 | g.23538561T>G | CA401792118 | NPC1 | c.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 |
18 | g.23538562A>C | CA503322455 | NPC1 | c.3021T>G (p.Pro1007=) c.2099T>G n.654T>G n.364T>G c.3072T>G (p.Pro1024=) c.2607T>G (p.Pro869=) | |
18 | g.23538562A>G | CA503322456 | NPC1 | c.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 |
18 | g.23538562A>T | CA503322457 | NPC1 | c.3021T>A (p.Pro1007=) c.2099T>A n.654T>A n.364T>A c.3072T>A (p.Pro1024=) c.2607T>A (p.Pro869=) | |
18 | g.23538563G>A | CA8912895 | NPC1 | c.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 |
18 | g.23538563G>C | CA401792119 | NPC1 | c.3020C>G (p.Pro1007Arg) c.2098C>G n.653C>G n.363C>G c.3071C>G (p.Pro1024Arg) c.2606C>G (p.Pro869Arg) | |
18 | g.23538563G= | CA2290165351 | NPC1 | c.3020C= (p.Pro1007=) c.2098C= n.653C= n.363C= c.3071C= (p.Pro1024=) c.2606C= (p.Pro869=) | |
18 | g.23538563G>T | CA401792120 | NPC1 | c.3020C>A (p.Pro1007His) c.2098C>A n.653C>A n.363C>A c.3071C>A (p.Pro1024His) c.2606C>A (p.Pro869His) | |
18 | g.23538564G>A | CA401792121 | NPC1 | c.3019C>T (p.Pro1007Ser) c.2097C>T n.652C>T n.362C>T c.3070C>T (p.Pro1024Ser) c.2605C>T (p.Pro869Ser) | |
18 | g.23538564G>C | CA340032 | NPC1 | c.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 |
18 | g.23538564G= | CA2290165352 | NPC1 | c.3019C= (p.Pro1007=) c.2097C= n.652C= n.362C= c.3070C= (p.Pro1024=) c.2605C= (p.Pro869=) | |
18 | g.23538564G>T | CA401792122 | NPC1 | c.3019C>A (p.Pro1007Thr) c.2097C>A n.652C>A n.362C>A c.3070C>A (p.Pro1024Thr) c.2605C>A (p.Pro869Thr) | |
18 | g.23538565G>A | CA503322458 | NPC1 | c.3018C>T (p.Asn1006=) c.2096C>T n.651C>T n.361C>T c.3069C>T (p.Asn1023=) c.2604C>T (p.Asn868=) | |
18 | g.23538565G>C | CA401792123 | NPC1 | c.3018C>G (p.Asn1006Lys) c.2096C>G n.651C>G n.361C>G c.3069C>G (p.Asn1023Lys) c.2604C>G (p.Asn868Lys) | |
18 | g.23538565G>T | CA401792124 | NPC1 | c.3018C>A (p.Asn1006Lys) c.2096C>A n.651C>A n.361C>A c.3069C>A (p.Asn1023Lys) c.2604C>A (p.Asn868Lys) | |
18 | g.23538566T>A | CA401792126 | NPC1 | c.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 |
18 | g.23538566T>C | CA401792127 | NPC1 | c.3017A>G (p.Asn1006Ser) c.2095A>G n.650A>G n.360A>G c.3068A>G (p.Asn1023Ser) c.2603A>G (p.Asn868Ser) | |
18 | g.23538566T>G | CA401792125 | NPC1 | c.3017A>C (p.Asn1006Thr) c.2095A>C n.650A>C n.360A>C c.3068A>C (p.Asn1023Thr) c.2603A>C (p.Asn868Thr) | dbSNP |
18 | g.23538566T= | CA2290165353 | NPC1 | c.3017A= (p.Asn1006=) c.2095A= n.650A= n.360A= c.3068A= (p.Asn1023=) c.2603A= (p.Asn868=) | |
18 | g.23538567del | CA2580095497 | NPC1 | c.3017del (p.Asn1006ThrfsTer?) c.2095del n.650del n.360del c.3068del (p.Asn1023ThrfsTer?) c.2603del (p.Asn868ThrfsTer?) | ClinVar |
18 | g.23538567T>A | CA401792128 | NPC1 | c.3016A>T (p.Asn1006Tyr) c.2094A>T n.649A>T n.359A>T c.3067A>T (p.Asn1023Tyr) c.2602A>T (p.Asn868Tyr) | |
18 | g.23538567T>C | CA401792130 | NPC1 | c.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 |
18 | g.23538567T>G | CA401792129 | NPC1 | c.3016A>C (p.Asn1006His) c.2094A>C n.649A>C n.359A>C c.3067A>C (p.Asn1023His) c.2602A>C (p.Asn868His) | |
18 | g.23538568A>C | CA401792131 | NPC1 | c.3015T>G (p.Asp1005Glu) c.2093T>G n.648T>G n.358T>G c.3066T>G (p.Asp1022Glu) c.2601T>G (p.Asp867Glu) | |
18 | g.23538568A>G | CA503322459 | NPC1 | c.3015T>C (p.Asp1005=) c.2093T>C n.648T>C n.358T>C c.3066T>C (p.Asp1022=) c.2601T>C (p.Asp867=) | |
18 | g.23538568A>T | CA401792132 | NPC1 | c.3015T>A (p.Asp1005Glu) c.2093T>A n.648T>A n.358T>A c.3066T>A (p.Asp1022Glu) c.2601T>A (p.Asp867Glu) | |
18 | g.23538569T>A | CA401792133 | NPC1 | c.3014A>T (p.Asp1005Val) c.2092A>T n.647A>T n.357A>T c.3065A>T (p.Asp1022Val) c.2600A>T (p.Asp867Val) | |
18 | g.23538569T>C | CA401792134 | NPC1 | c.3014A>G (p.Asp1005Gly) c.2092A>G n.647A>G n.357A>G c.3065A>G (p.Asp1022Gly) c.2600A>G (p.Asp867Gly) | |
18 | g.23538569T>G | CA401792135 | NPC1 | c.3014A>C (p.Asp1005Ala) c.2092A>C n.647A>C n.357A>C c.3065A>C (p.Asp1022Ala) c.2600A>C (p.Asp867Ala) | |
18 | g.23538570C>A | CA401792136 | NPC1 | c.3013G>T (p.Asp1005Tyr) c.2091G>T n.646G>T n.356G>T c.3064G>T (p.Asp1022Tyr) c.2599G>T (p.Asp867Tyr) | |
18 | g.23538570C>G | CA401792137 | NPC1 | c.3013G>C (p.Asp1005His) c.2091G>C n.646G>C n.356G>C c.3064G>C (p.Asp1022His) c.2599G>C (p.Asp867His) | |
18 | g.23538570C>T | CA401792138 | NPC1 | c.3013G>A (p.Asp1005Asn) c.2091G>A n.646G>A n.356G>A c.3064G>A (p.Asp1022Asn) c.2599G>A (p.Asp867Asn) | |
18 | g.23538571C>A | CA503322460 | NPC1 | c.3012G>T (p.Ser1004=) c.2090G>T n.645G>T n.355G>T c.3063G>T (p.Ser1021=) c.2598G>T (p.Ser866=) | |
18 | g.23538571C= | CA2290165354 | NPC1 | c.3012G= (p.Ser1004=) c.2090G= n.645G= n.355G= c.3063G= (p.Ser1021=) c.2598G= (p.Ser866=) | |
18 | g.23538571C>G | CA503322461 | NPC1 | c.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 |
18 | g.23538571C>T | CA8912896 | NPC1 | c.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 |
18 | g.23538572G>A | CA8912897 | NPC1 | c.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 |
18 | g.23538572G>C | CA401792140 | NPC1 | c.3011C>G (p.Ser1004Trp) c.2089C>G n.644C>G n.354C>G c.3062C>G (p.Ser1021Trp) c.2597C>G (p.Ser866Trp) | |
18 | g.23538572G= | CA2290165355 | NPC1 | c.3011C= (p.Ser1004=) c.2089C= n.644C= n.354C= c.3062C= (p.Ser1021=) c.2597C= (p.Ser866=) | |
18 | g.23538572G>T | CA401792139 | NPC1 | c.3011C>A (p.Ser1004Ter) c.2089C>A n.644C>A n.354C>A c.3062C>A (p.Ser1021Ter) c.2597C>A (p.Ser866Ter) | |
18 | g.23538573A>C | CA401792141 | NPC1 | c.3010T>G (p.Ser1004Ala) c.2088T>G n.643T>G n.353T>G c.3061T>G (p.Ser1021Ala) c.2596T>G (p.Ser866Ala) | |
18 | g.23538573A>G | CA401792142 | NPC1 | c.3010T>C (p.Ser1004Pro) c.2088T>C n.643T>C n.353T>C c.3061T>C (p.Ser1021Pro) c.2596T>C (p.Ser866Pro) | |
18 | g.23538573A>T | CA401792143 | NPC1 | c.3010T>A (p.Ser1004Thr) c.2088T>A n.643T>A n.353T>A c.3061T>A (p.Ser1021Thr) c.2596T>A (p.Ser866Thr) | |
18 | g.23538574A>C | CA503322462 | NPC1 | c.3009T>G (p.Leu1003=) c.2087T>G n.642T>G n.352T>G c.3060T>G (p.Leu1020=) c.2595T>G (p.Leu865=) | |
18 | g.23538574A>G | CA503322463 | NPC1 | c.3009T>C (p.Leu1003=) c.2087T>C n.642T>C n.352T>C c.3060T>C (p.Leu1020=) c.2595T>C (p.Leu865=) | |
18 | g.23538574A>T | CA503322464 | NPC1 | c.3009T>A (p.Leu1003=) c.2087T>A n.642T>A n.352T>A c.3060T>A (p.Leu1020=) c.2595T>A (p.Leu865=) | |
18 | g.23538575A>C | CA401792144 | NPC1 | c.3008T>G (p.Leu1003Arg) c.2086T>G n.641T>G n.351T>G c.3059T>G (p.Leu1020Arg) c.2594T>G (p.Leu865Arg) |