Variant #0001056755 (NC_000019.9:g.50728876C>A, NM_024729.3:c.728C>A (MYH14))
| Chromosome |
19 |
| 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.50728876C>A |
| DNA change (hg38) |
- |
| Published as |
MYH14(NM_001145809.1):c.752C>A (p.P251H), MYH14(NM_001145809.2):c.752C>A (p.P251H, p.(Pro251His)) |
| ISCN |
- |
| DB-ID |
MYH14_000020 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) |
3.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-11-01 13:22:20 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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