Variant #0000016107 (NC_000017.10:g.57134269T>C, NM_015294.3:c.1166A>G (TRIM37))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57134269T>C |
| DNA change (hg38) |
g.59056908T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TRIM37_000018 |
| Variant remarks |
1 Finnish MUL patient (com-het) |
| Reference |
Hämäläinen, Lipsanen-Nyman, Lehesjoki, unpublished data |
| ClinVar ID |
- |
| dbSNP ID |
rs312262705 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/95 CEPH |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-09-25 14:35:54 +02:00 (CEST) |
| Date last edited |
2017-05-05 18:33:04 +02:00 (CEST) |

Variant on transcripts
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