Variant #0000679617 (NC_000012.11:g.6127833T>C, NM_000552.3:c.4751A>G (VWF))
| Chromosome |
12 |
| 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.6127833T>C |
| DNA change (hg38) |
- |
| Published as |
VWF(NM_000552.3):c.4751A>G (p.Y1584C, p.(Tyr1584Cys)), VWF(NM_000552.4):c.4751A>G (p.Y1584C), VWF(NM_000552.5):c.4751A>G (p.Y1584C) |
| ISCN |
- |
| DB-ID |
VWF_000117 See all 22 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) |
0.00271 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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