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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