Variant #0000039758 (NC_000009.11:g.35658039_35658040insGAGGAGTAGT, NR_003051.3:n.-18_-17insCTCACTACTC (RMRP))
| Chromosome |
9 |
| Allele |
Maternal (confirmed) |
| 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.35658039_35658040insGAGGAGTAGT |
| DNA change (hg38) |
g.35658042_35658043insGAGGAGTAGT |
| Published as |
M29916.1: g.726_727insCTCACTACTC |
| ISCN |
- |
| DB-ID |
RMRP_000103 |
| Variant remarks |
1 patient with CHH (com-het); 10-nucleotide insertion at position -18 in the promoter region of the RMRP gene |
| Reference |
PubMed: Crahes et al. 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| 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 |
2014-07-26 19:52:33 +02:00 (CEST) |
| Date last edited |
2020-06-25 13:39:12 +02:00 (CEST) |

Variant on transcripts
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