Variant #0000525422 (NC_000005.9:g.179260655G>A, NM_003900.4:c.1038G>A (SQSTM1))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179260655G>A |
DNA change (hg38) |
g.179833655G>A |
Published as |
SQSTM1(NM_003900.5):c.1038G>A (p.V346=) |
ISCN |
- |
DB-ID |
C5orf45_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) |
0.0002 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-06-18 11:25:41 +02:00 (CEST) |

Variant on transcripts
|