Variant #0000913267 (NC_000010.10:g.26315400C>T, NM_017433.4:c.892C>T (MYO3A))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.26315400C>T |
| DNA change (hg38) |
- |
| Published as |
MYO3A(NM_017433.5):c.892C>T (p.Q298*) |
| ISCN |
- |
| DB-ID |
MYO3A_000101 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00012 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2023-01-11 15:44:22 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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