Variant #0000324631 (NC_000016.9:g.15931893T>G, NM_001040113.1:c.217A>C (MYH11))
| Chromosome |
16 |
| 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.15931893T>G |
| DNA change (hg38) |
g.15838036T>G |
| Published as |
MYH11(NM_001040113.1):c.217A>C (p.(Lys73Gln)), MYH11(NM_001040113.2):c.217A>C (p.K73Q), MYH11(NM_002474.3):c.217A>C (p.K73Q) |
| ISCN |
- |
| DB-ID |
MYH11_000132 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) |
0.00031 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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