Variant #0000536301 (NC_000009.11:g.130425578A>C, NM_003165.3:c.524A>C (STXBP1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.130425578A>C |
DNA change (hg38) |
g.127663299A>C |
Published as |
- |
ISCN |
- |
DB-ID |
STXBP1_000115 |
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 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
|