Variant #0000016192 (NC_000009.11:g.35658028_35658034dup, NR_003051.3:n.-19_-13dupTCTGTGA (RMRP))
| Chromosome |
9 |
| 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.35658028_35658034dup |
| DNA change (hg38) |
g.35658031_35658037dup |
| Published as |
dup TCTGTGA at -13; g.-20_-14dupTCTGTGA; -14_-20dupTCTGTGA; -20-14dup |
| ISCN |
- |
| DB-ID |
RMRP_000011 |
| Variant remarks |
2 American CHH families, 1 American CHH patient and 1 CHH family with undetermined ethnicity (all com-het) |
| Reference |
PubMed: Ridanpää et al. 2002, PubMed: Bonafe et al. 2005, PubMed: Hermanns el al. 2006, PubMed: Kavadas et al. 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/280 CON |
| 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 11:57:12 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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