Variant #0000555505 (NC_000015.9:g.75673984_75673986del, NM_001145358.1:c.3259_3261del (SIN3A))
Chromosome |
15 |
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.75673984_75673986del |
DNA change (hg38) |
g.75381643_75381645del |
Published as |
SIN3A(NM_001145358.1):c.3259_3261del (p.(Glu1087del)) |
ISCN |
- |
DB-ID |
SIN3A_000012 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
|