Variant #0000953831 (NC_000018.9:g.21119429C>T, NM_000271.4:c.2801G>A (NPC1))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21119429C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NPC1_000270 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs786204714
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-12-20 14:40:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPC1 NM_000271.4 +?/. - c.2801G>A r.(?) p.(Arg934Gln)


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