Variant #0000021396 (NC_000022.10:g.36692955_36692975del, NM_002473.4:c.3195_3215del (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.36692955_36692975del
DNA change (hg38) g.36296909_36296929del
Published as -
ISCN -
DB-ID MYH9_000012 See all 2 reported entries
Variant remarks -
Reference PubMed: Pecci 2008
ClinVar ID -
dbSNP ID -
Origin De novo
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 16:45:57 +02:00 (CEST)
Date last edited 2020-07-17 12:20:53 +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 +/. 25 c.3195_3215del r.(?) p.(Gln1066_Ala1072del)


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