Variant #0001063302 (NC_000001.10:g.231402086G>T, NM_014236.3:c.988G>T (GNPAT))

Chromosome 1
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.231402086G>T
DNA change (hg38) -
Published as GNPAT(NM_014236.4):c.988G>T (p.(Asp330Tyr))
ISCN -
DB-ID C1orf131_000028
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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     
GNPAT NM_014236.3 ?/. - c.988G>T r.(?) p.(Asp330Tyr)
C1orf131 NM_152379.2 ?/. - c.-25199C>A r.(?) p.(=)


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