Variant #0000016199 (NC_000009.11:g.35658011G>A, NR_003051.3:n.5C>T (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.35658011G>A |
| DNA change (hg38) |
g.35658014G>A |
| Published as |
4T; g.4C>T; 4C>T |
| ISCN |
- |
| DB-ID |
RMRP_000018 |
| Variant remarks |
1 Australian, 1 Dutch, 1 English, 1 German, 1 Spanish, 1 Swiss and 1 Italian CHH family, 1 German CHH patient and 2 CHH patients and 1 CHH family with undetermined ethnicity (all com-het) |
| Reference |
PubMed: Ridanpää et al. 2002, PubMed: Bonafe 2005, PubMed: Roifman 2006, PubMed: Hermanns 2006, PubMed: Munoz-Robles 2006 and PubMed: Kavadas 2008, PubMed: Bacchetta 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/280 CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00011 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-07 13:32:46 +01:00 (CET) |
| Date last edited |
2020-06-25 13:30:02 +02:00 (CEST) |

Variant on transcripts
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