Variant #0000981642 (NC_000016.9:g.15917142C>T, NM_001040113.1:c.472G>A (MYH11))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15917142C>T |
| DNA change (hg38) |
- |
| Published as |
MYH11(NM_001040113.1):c.472G>A (p.A158T), MYH11(NM_001040113.2):c.472G>A (p.A158T), MYH11(NM_002474.3):c.472G>A (p.A158T) |
| ISCN |
- |
| DB-ID |
MYH11_000209 See all 4 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_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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