Variant #0000948010 (NC_000003.11:g.12458374A>G, NM_005037.5:c.907A>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.12458374A>G
DNA change (hg38) -
Published as PPARG(NM_015869.4):c.991A>G (p.(Ile331Val))
ISCN -
DB-ID PPARG_000044
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) 3.0E-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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPARG NM_005037.5 ?/. - c.907A>G r.(?) p.(Ile303Val)
PPARG NM_138711.3 ?/. - c.907A>G r.(?) p.(Ile303Val)


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