Variant #0000791084 (NC_000001.10:g.17380479del, SDHB(NM_003000.2):c.36del)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
other |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17380479del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
SDHB_000398 |
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 |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Jean-Pierre Bayley |
Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
Created by |
Jean-Pierre Bayley |

Variant on transcripts
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