Variant #0000342264 (NC_000001.10:g.17349219G>A, NM_003000.2:c.649C>T (SDHB))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17349219G>A
DNA change (hg38) g.17022724G>A
Published as SDHB(NM_003000.3):c.649C>T (p.R217C)
ISCN -
DB-ID SDHB_000086 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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 +/+? - c.649C>T p.(Arg217Cys) missense r.(?) -


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