Variant #0000441278 (NC_000003.11:g.189582249G>A, NC_000003.11(NM_003722.4):c.766+42G>A (TP63))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.189582249G>A |
| DNA change (hg38) |
g.189864460G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TP63_000008 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2276792 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.12329 View details |
| Owner |
Paul van der Zwaag |
| Database submission license |
No license selected |
| Created by |
Paul van der Zwaag |
| Date created |
2009-02-25 11:22:42 +01:00 (CET) |
| Date last edited |
2018-12-23 11:56:15 +01:00 (CET) |

Variant on transcripts
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