Variant #0000339541 (NC_000001.10:g.17380491G>A, SDHB(NM_003000.2):c.24C>T)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17380491G>A |
DNA change (hg38) |
g.17053996G>A |
Published as |
SDHB(NM_003000.2):c.24C>T (p.S8=, p.(Ser8=)) |
ISCN |
- |
DB-ID |
SDHB_000011 See all 7 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00437 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |

Variant on transcripts
|
|