Variant #0000905538 (NC_000002.11:g.71681133T>C, NM_003494.3:c.5T>C (DYSF))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71681133T>C |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
DYSF_001406 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1243373795 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2022-12-02 11:29:01 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|