Variant #0000564198 (NC_000018.9:g.21140411T>C, NM_000271.4:c.665A>G (NPC1))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21140411T>C
DNA change (hg38) g.23560447T>C
Published as NPC1(NM_000271.4):c.665A>G (p.N222S), NPC1(NM_000271.5):c.665A>G (p.N222S)
ISCN -
DB-ID NPC1_000001 See all 9 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00333 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPC1 NM_000271.4 ?/. - c.665A>G r.(?) p.(Asn222Ser)


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