Transcript #00013071 (NM_000271.4, NPC1 gene)

Transcript name Niemann-Pick disease, type C1
Gene name NPC1 (Niemann-Pick disease, type C1)
Chromosome 18
Transcript - NCBI ID NM_000271.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000262.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

265 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.-22A>C -22 r.(=) p.(=) - utr-5 -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.387T>C 387 r.(?) p.(=) - coding-synonymous -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.644A>G 644 r.(?) p.(His215Arg) - missense -
./. - c.709C>T 709 r.(?) p.(Pro237Ser) - missense -
./. - c.966C>T 966 r.(?) p.(=) - coding-synonymous -
./. - c.1503C>T 1503 r.(?) p.(=) - coding-synonymous -
./. - c.1532C>T 1532 r.(?) p.(Thr511Met) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1926G>C 1926 r.(?) p.(Met642Ile) - missense -
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+12_1947+13insAGGG 1947 r.(=) p.(=) - intron 12
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.1947+14G>T 1947 r.(=) p.(=) - intron 14
./. - c.2103C>T 2103 r.(?) p.(=) - coding-synonymous -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
./. - c.2572A>G 2572 r.(?) p.(Ile858Val) - missense -
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