Variant #0000553000 (NC_000014.8:g.74953134C>T, NM_006432.3:c.88G>A (NPC2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74953134C>T
DNA change (hg38) g.74486431C>T
Published as NPC2(NM_006432.4):c.88G>A (p.V30M), NPC2(NM_006432.5):c.88G>A (p.V30M)
ISCN -
DB-ID NPC2_000001 See all 7 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) 0.0022 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPC2 NM_006432.3 -?/. - c.88G>A r.(?) p.(Val30Met)


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