Variant #0000445606 (NC_000014.8:g.23901866A>G, MYH7(NM_000257.2):c.484T>C)

Individual ID 00212621
Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23901866A>G
DNA change (hg38) g.23432657A>G
Published as -
ISCN -
DB-ID MYH7_000057
Variant remarks -
Reference PubMed: Meder 2011
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 +?/. 5 c.484T>C r.(?) p.(Tyr162His)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000213697 DNA SEQ - - MYH7 1 Johan den Dunnen