Variant #0001063878 (NC_000003.11:g.12458335G>A, NM_005037.5:c.868G>A (PPARG))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.12458335G>A
DNA change (hg38) -
Published as PPARG(NM_015869.4):c.952G>A (p.(Val318Met)), PPARG(NM_015869.5):c.952G>A (p.V318M)
ISCN -
DB-ID PPARG_000016 See all 3 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 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     
PPARG NM_005037.5 +/. - c.868G>A r.(?) p.(Val290Met)
PPARG NM_138711.3 +/. - c.868G>A r.(?) p.(Val290Met)


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