Variant #0000021364 (NC_000022.10:g.36680520C>T, NM_002473.4:c.5521G>A (MYH9))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36680520C>T |
| DNA change (hg38) |
g.36284474C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MYH9_000026 See all 16 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Pecci 2008, PubMed: Savoia 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anna Savoia |
| Database submission license |
No license selected |
| Created by |
Anna Savoia |
| Date created |
2013-10-04 14:40:18 +02:00 (CEST) |
| Date last edited |
2019-05-17 12:32:51 +02:00 (CEST) |

Variant on transcripts
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