Variant #0000788746 (NC_000001.10:g.17349219G>A, NM_003000.2:c.649C>T (SDHB))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method other
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17349219G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHB_000086 See all 5 reported entries
Variant remarks Variant classified by experts from the NGSnPPGL study group (ENS@T/PRESSOR)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
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 2021-06-10 17:26:40 +02:00 (CEST)
Date last edited 2021-06-29 10:16:41 +02:00 (CEST)
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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 +?/+? 7 c.649C>T p.(Arg217Cys) missense r.(?) -


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