Variant #0000258402 (NC_000009.11:g.119460297C>T, NM_012210.3:c.276C>T (TRIM32))
| 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.119460297C>T |
| DNA change (hg38) |
g.116698018C>T |
| Published as |
ASTN2(NM_014010.5):c.2653+27753G>A, TRIM32(NM_001099679.1):c.276C>T (p.(Ser92=)), TRIM32(NM_012210.3):c.276C>T (p.S92=), TRIM32(NM_012210.4):c.276C... |
| ISCN |
- |
| DB-ID |
TRIM32_000023 See all 3 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) |
0.00024 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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