Variant #0001067834 (NC_000011.9:g.111958676C>G, NM_003002.2:c.148C>G (SDHD))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111958676C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHD_000209 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Jean-Pierre Bayley
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Jean-Pierre Bayley
Date created 2026-01-21 10:25:03 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Predicted     

RNA change     

Predict-BioInf     
SDHD NM_003002.2 +?/-? 1 c.148C>G p.(His50Asp) missense r.(?) -


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