Variant #0000021395 (NC_000022.10:g.36678800G>A, NM_002473.4:c.5797C>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.36678800G>A
DNA change (hg38) g.36282754G>A
Published as -
ISCN -
DB-ID MYH9_000030 See all 21 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) 0 View details
Owner Anna Savoia
Database submission license No license selected
Created by Anna Savoia
Date created 2013-10-04 16:35:42 +02:00 (CEST)
Date last edited 2019-05-17 12:32:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH9 NM_002473.4 +/. 41 c.5797C>T r.(?) p.(Arg1933*)


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