Variant #0000928694 (NC_000003.11:g.12422941A>G, NM_005037.5:c.347A>G (PPARG))

Chromosome 3
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.12422941A>G
DNA change (hg38) -
Published as PPARG(NM_001330615.1):c.347A>G (p.(Asp116Gly)), PPARG(NM_001354668.2):c.431A>G (p.D144G)
ISCN -
DB-ID PPARG_000039 See all 2 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPARG NM_005037.5 ?/. - c.347A>G r.(?) p.(Asp116Gly)
PPARG NM_138711.3 ?/. - c.347A>G r.(?) p.(Asp116Gly)


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