Variant #0000314821 (NC_000009.11:g.119460542C>T, NM_012210.3:c.521C>T (TRIM32))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119460542C>T |
| DNA change (hg38) |
g.116698263C>T |
| Published as |
TRIM32(NM_001099679.1):c.521C>T (p.(Ser174Phe)), TRIM32(NM_012210.3):c.521C>T (p.S174F), TRIM32(NM_012210.4):c.521C>T (p.S174F) |
| ISCN |
- |
| DB-ID |
TRIM32_000029 See all 7 reported entries |
| 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) |
0.00019 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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