Variant #0000001497 (NC_000017.10:g.57161406C>G, NM_015294.3:c.326G>C (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.57161406C>G |
DNA change (hg38) |
g.59084045C>G |
Published as |
- |
ISCN |
- |
DB-ID |
TRIM37_000001 |
Variant remarks |
1 Australian MUL patient (com-het) |
Reference |
PubMed: Hämäläinen et al. 2006 |
ClinVar ID |
- |
dbSNP ID |
rs121908391 |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Anne Polvi |
Database submission license |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-08-29 11:18:58 +02:00 (CEST) |
Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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