Variant #0000644084 (NC_000014.8:g.77920368G>A, NM_022067.3:c.78C>T (VIPAS39))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77920368G>A |
| DNA change (hg38) |
g.77454025G>A |
| Published as |
c.2T>G (p.(Met1Arg)) |
| ISCN |
- |
| DB-ID |
VIPAS39_000010 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs112217896 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
6.0E-5 View details |
| Owner |
Paul Gissen |
| Database submission license |
No license selected |
| Created by |
Paul Gissen |
| Date created |
2011-08-22 13:28:12 +02:00 (CEST) |
| Date last edited |
2021-09-09 14:41:03 +02:00 (CEST) |

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