Variant #0000788308 (NC_000001.10:g.17359572C>T, NM_003000.2:c.269G>A (SDHB))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method other
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.17359572C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SDHB_000099 See all 4 reported entries
Variant remarks Variant classified by experts from the NGSnPPGL study group (ENS@T/PRESSOR). Align GVGD: Class C65 (most likely to affect function). Similar AAs but Asn uncharged. Highly conserved, in highly conserved region close to 2FE-2S binding site. Medium to low Grantham score (86). VUS
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 2021-06-03 23:16:20 +02:00 (CEST)
Date last edited 2023-01-25 11:01:10 +01:00 (CET)
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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 ?/? 3 c.269G>A p.(Arg90Gln) missense r.(?) SIFT 0.00


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