Variant #0000858779 (NC_000003.11:g.12434142G>C, NM_005037.5:c.426G>C (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.12434142G>C
DNA change (hg38) -
Published as PPARG(NM_001330615.1):c.426G>C (p.(Lys142Asn))
ISCN -
DB-ID PPARG_000023
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 2022-05-09 15:51:19 +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.426G>C r.(?) p.(Lys142Asn)
PPARG NM_138711.3 ?/. - c.426G>C r.(?) p.(Lys142Asn)


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