Variant #0001057214 (NC_000022.10:g.46643007C>T, NM_001001928.2:c.*11730C>T (PPARA))

Chromosome 22
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.46643007C>T
DNA change (hg38) -
Published as CDPF1(NM_207327.5):c.225G>A (p.(Pro75=))
ISCN -
DB-ID PPARA_000002
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 2025-11-01 13:22:20 +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     
PPARA NM_001001928.2 ?/. - c.*11730C>T r.(=) p.(=)
CDPF1 NM_207327.4 ?/. - c.225G>A r.(?) p.(=)


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