Variant #0000522811 (NC_000004.11:g.6290807_6290822dup, NM_006005.3:c.409_424dup (WFS1))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6290807_6290822dup |
DNA change (hg38) |
g.6289080_6289095dup |
Published as |
WFS1(NM_006005.3):c.409_424dupGGCCGTCGCGAGGCTG (p.(Val142fs)), WFS1(NM_006005.3):c.409_424dupGGCCGTCGCGAGGCTG (p.V142Gfs*110) |
ISCN |
- |
DB-ID |
WFS1_000403 See all 4 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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