Variant #0000925067 (NC_000009.11:g.73255510C>T, NM_206945.3:c.953G>A (TRPM3))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.73255510C>T |
| DNA change (hg38) |
- |
| Published as |
TRPM3(NM_001366147.2):c.1487G>A (p.R496H) |
| ISCN |
- |
| DB-ID |
TRPM3_000035 |
| 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|