Variant #0000016194 (NC_000009.11:g.35658027_35658028insCACAGAT, NR_003051.3:n.-13_-12insATCTGTG (RMRP))
| Chromosome |
9 |
| Allele |
Maternal (confirmed) |
| 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.35658027_35658028insCACAGAT |
| DNA change (hg38) |
g.35658030_35658031insCACAGAT |
| Published as |
insertion ATCTGTG at -13 |
| ISCN |
- |
| DB-ID |
RMRP_000013 |
| Variant remarks |
1 CHH patient with undetermined ethnicity (com-het) |
| Reference |
PubMed: Roifman et al. 2006 |
| 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 |
2012-11-07 13:05:36 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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