Variant #0000839545 (NC_000002.11:g.71896721A>G, NC_000002.11(NM_003494.3):c.5526-14A>G (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.71896721A>G |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
DYSF_001143 See all 3 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1215271482 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2022-02-09 12:13:01 +01:00 (CET) |
Date last edited |
2022-09-26 12:22:42 +02:00 (CEST) |

Variant on transcripts
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