Variant #0000530417 (NC_000007.13:g.108113027G>A, NM_015723.3:c.2167C>T (PNPLA8))

Chromosome 7
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.108113027G>A
DNA change (hg38) g.108472583G>A
Published as PNPLA8(NM_015723.4):c.2167C>T (p.R723*)
ISCN -
DB-ID PNPLA8_000003
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNPLA8 NM_001256007.2 ?/. - c.2167C>T r.(?) p.(Arg723Ter)
PNPLA8 NM_015723.3 ?/. - c.2167C>T r.(?) p.(Arg723Ter)


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