Variant #0000331963 (NC_000007.13:g.150721489C>G, NM_000603.4:c.*10232C>G (NOS3))
Chromosome |
7 |
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.150721489C>G |
DNA change (hg38) |
g.151024402C>G |
Published as |
ATG9B(NM_173681.5):c.22G>C (p.(Gly8Arg)) |
ISCN |
- |
DB-ID |
ATG9B_000001 |
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) |
0.0016 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-23 15:00:12 +02:00 (CEST) |

Variant on transcripts
|