Variant #0000644089 (NC_000014.8:g.77896048C>T, NM_022067.3:c.1242G>A (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.77896048C>T |
| DNA change (hg38) |
g.77429705C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
VIPAS39_000014 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs45447095 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
0.0053 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00589 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
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