Variant #0001022228 (NC_000017.10:g.10304362C>T, NC_000017.10(NM_002472.2):c.3254+1G>A (MYH8))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.10304362C>T |
| DNA change (hg38) |
g.10401045C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MYH8_000025 See all 3 reported entries |
| Variant remarks |
in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA inclusion of intron sequences |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00022 View details |
| Owner |
Tjakko van Ham |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-11-05 16:15:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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