Variant #0001060447 (NC_000011.9:g.35016549C>T, NM_003477.2:c.1336C>T (PDHX))

Chromosome 11
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.35016549C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PDHX_000016
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1135402725
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-12-03 09:14:01 +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     
PDHX NM_003477.2 +/. - c.1336C>T r.(?) p.(Arg446Ter)


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