Variant #0001022585 (NC_000017.10:g.57165714T>C, NM_015294.3:c.219A>G (TRIM37))
Chromosome |
17 |
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.57165714T>C |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TRIM37_000077 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2025-01-31 11:17:01 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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