Variant #0001031804 (NC_000001.10:g.231401904C>G, NM_014236.3:c.917C>G (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.231401904C>G
DNA change (hg38) -
Published as GNPAT(NM_014236.4):c.917C>G (p.(Ser306Cys))
ISCN -
DB-ID C1orf131_000022
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) 0.00011 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPAT NM_014236.3 ?/. - c.917C>G r.(?) p.(Ser306Cys)
C1orf131 NM_152379.2 ?/. - c.-25017G>C r.(?) p.(=)


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