Variant #0000717260 (NC_000001.10:g.231398584T>C, NM_014236.3:c.554T>C (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.231398584T>C
DNA change (hg38) -
Published as GNPAT(NM_001316350.1):c.371T>C (p.(Ile124Thr))
ISCN -
DB-ID C1orf131_000008
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) 1.0E-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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPAT NM_014236.3 ?/. - c.554T>C r.(?) p.(Ile185Thr)
C1orf131 NM_152379.2 ?/. - c.-21697A>G r.(?) p.(=)


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