Variant #0000016110 (NC_000017.10:g.57106034G>A, NM_015294.3:c.1999C>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.57106034G>A |
| DNA change (hg38) |
g.59028673G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TRIM37_000021 |
| Variant remarks |
1 Polish MUL patient (com-het) |
| Reference |
Kettunen, Pachucki, Lehesjoki unpublished data |
| ClinVar ID |
- |
| dbSNP ID |
rs312262702 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-09-26 14:03:37 +02:00 (CEST) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
|