Variant #0000445926 (NC_000014.8:g.23901922C>T, MYH7(NM_000257.2):c.428G>A)

Individual ID 00212936
Chromosome 14
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23901922C>T
DNA change (hg38) g.23432713C>T
Published as X52889.1:5410G>A
ISCN -
DB-ID MYH7_000054 See all 4 reported entries
Variant remarks -
Reference Koyanagi Circulation 1996 94:I84
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 +/. 5 c.428G>A r.(?) p.(Arg143Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000214012 DNA SEQ - - MYH7 1 Johan den Dunnen