Variant #0000001499 (NC_000017.10:g.57148248G>A, NM_015294.3:c.745C>T (TRIM37))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57148248G>A |
DNA change (hg38) |
g.59070887G>A |
Published as |
- |
ISCN |
- |
DB-ID |
TRIM37_000003 |
Variant remarks |
1 Canadian MUL patient (com-het) |
Reference |
PubMed: Hämäläinen et al. 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
0/85 CEPH |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Anne Polvi |
Database submission license |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-08-29 11:37:24 +02:00 (CEST) |
Date last edited |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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