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Hämäläinen, Lipsanen-Nyman, Lehesjoki, unpublished data |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 |
No license selected |
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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