Variant #0000021403 (NC_000022.10:g.36702031G>A, NM_002473.4:c.2104C>T (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.36702031G>A |
DNA change (hg38) |
g.36305985G>A |
Published as |
- |
ISCN |
- |
DB-ID |
MYH9_000006 See all 19 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 17:05:12 +02:00 (CEST) |
Date last edited |
2019-05-17 12:32:51 +02:00 (CEST) |

Variant on transcripts
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