Variant #0000010960 (NC_000014.8:-, MYH7(NM_000257.2):c.597A>G)

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type lymphocyte
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYH7_00016 See all 6 reported entries
Frequency 0.033
Variant remarks rs2069541
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 ./. 07 c.597A>G - p.Ala199Ala