Variant #0000016995 (NC_000009.11:g.35657924C>T, NR_003051.3:n.92G>A (RMRP))
| Chromosome |
9 |
| Allele |
Parent #1 |
| 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.35657924C>T |
| DNA change (hg38) |
g.35657927C>T |
| Published as |
91G>A |
| ISCN |
- |
| DB-ID |
RMRP_000058 |
| Variant remarks |
1 Belgian CHH patient (com-het); Variants n.91G>A and n.101C>T are in same haplotype and it is unclear which of them is (or both are) causative |
| Reference |
PubMed: Hermanns el 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 |
2013-01-30 15:07:13 +01:00 (CET) |
| Date last edited |
2020-06-25 13:28:18 +02:00 (CEST) |

Variant on transcripts
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