Variant #0000286958 (NC_000016.9:g.15808876C>G, NM_001040113.1:c.5697G>C (MYH11))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15808876C>G |
| DNA change (hg38) |
g.15715019C>G |
| Published as |
MYH11(NM_001040113.1):c.5697G>C (p.E1899D), MYH11(NM_001040113.2):c.5697G>C (p.E1899D), MYH11(NM_002474.3):c.5676G>C (p.(Glu1892Asp), p.E1892D), ND... |
| ISCN |
- |
| DB-ID |
MYH11_000014 See all 6 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) |
0.00502 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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