Variant #0001048779 (NC_000001.10:g.17380483C>T, NM_003000.2:c.32G>A (SDHB))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17380483C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHB_000141 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs111430410
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00036 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-08 18:15:02 +02:00 (CEST)
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     
SDHB NM_003000.2 -?/. - c.32G>A p.(Arg11His) - r.(?) -


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