Variant #0001067860 (NC_000011.9:g.111957684G>T, NC_000011.9(NM_003002.2):c.52+1G>T (SDHD))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.111957684G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHD_000232
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 14:04:01 +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 +?/+? - c.52+1G>T p.? splicing affected? r.spl? -


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