Variant #0000858658 (NC_000002.11:g.71801344_71801349dup, NM_003494.3:c.3191_3196dup (DYSF))
Chromosome |
2 |
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.71801344_71801349dup |
DNA change (hg38) |
- |
Published as |
DYSF(NM_001130455.1):c.3194_3199dup (p.(Ala1065_Glu1066dup)), DYSF(NM_001130981.2):c.3242_3247dupCGGAGG (p.A1081_E1082dup) |
ISCN |
- |
DB-ID |
DYSF_000112 See all 32 reported entries |
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 |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|