Variant #0000016154 (NC_000009.11:g.35657945T>C, NR_003051.3:n.71A>G (RMRP))
| Chromosome |
9 |
| Allele |
Unknown |
| 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.35657945T>C |
| DNA change (hg38) |
g.35657948T>C |
| Published as |
70A>G |
| ISCN |
- |
| DB-ID |
RMRP_000005 See all 4 reported entries |
| Variant remarks |
Finnish Major CHH mutation, (90> Finnish CHH families; most homozygous), and also the most common mutation (~48%) in other countries: Observed in American (also Amish), Australian, Austrian, Belgian, Brazilian, Canadian, Dutch, English, French, German, Turkish, Irish and Mexican CHH patients |
| Reference |
PubMed: Ridanpää et al. 2001&PubMed: 2002, PubMed: Bonafe et al. 2002&PubMed: 2005 and others PubMed: 2006, PubMed: 2008, PubMed: 2011, PubMed: 2012, PubMed: 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
10/845 FIN CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00088 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-05 10:15:58 +01:00 (CET) |
| Date last edited |
2020-06-25 13:28:20 +02:00 (CEST) |

Variant on transcripts
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