Variant #0000016978 (NC_000009.11:g.35658004T>C, NR_003051.3:n.12A>G (RMRP))
| Chromosome |
9 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35658004T>C |
| DNA change (hg38) |
g.35658007T>C |
| Published as |
g.11A>G reported previously as polymorphisms |
| ISCN |
- |
| DB-ID |
RMRP_000041 |
| Variant remarks |
- |
| Reference |
PubMed: Kwan et al. 2012 |
| 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 13:30:01 +02:00 (CEST) |

Variant on transcripts
|