Variant #0000536132 (NC_000009.11:g.119460579G>C, NM_012210.3:c.558G>C (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.119460579G>C |
DNA change (hg38) |
g.116698300G>C |
Published as |
ASTN2(NM_014010.5):c.2653+27471C>G, TRIM32(NM_001099679.1):c.558G>C (p.Q186H, p.(Gln186His)), TRIM32(NM_012210.3):c.558G>C (p.Q186H), TRIM32(NM_01...) |
ISCN |
- |
DB-ID |
TRIM32_000030 See all 17 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) |
0.0019 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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