Variant #0000670106 (NC_000023.10:g.19375782A>C, PDHA1(NM_000284.3):c.844A>C)

Individual ID 00305289
Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19375782A>C
DNA change (hg38) g.19357664A>C
Published as -
ISCN -
DB-ID PDHA1_000022 See all 4 reported entries
Variant remarks 19 homozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs2229137
Origin Germline
Segregation -
Frequency 19/2793 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02049 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDHA1 NM_000284.3 -/. - c.844A>C r.(?) p.(Met282Leu)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000306418 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq