Variant #0000441297 (NC_000003.11:g.189526027C>T, NC_000003.11(NM_003722.4):c.325-34C>T (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.189526027C>T |
| DNA change (hg38) |
g.189808238C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TP63_000003 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs36023188 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00144 View details |
| Owner |
Paul van der Zwaag |
| Database submission license |
No license selected |
| Created by |
Paul van der Zwaag |
| Date created |
2009-02-25 11:17:57 +01:00 (CET) |
| Date last edited |
2025-06-08 20:04:09 +02:00 (CEST) |

Variant on transcripts
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