Variant #0000011515 (NC_000012.11:-, MYL2(NM_000432.3):c.132T>C)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Blood
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00012
Frequency -
Variant remarks Five more frequent SNPs were located in the exon flanking regions of introns 4 and 5 of MYL2 (three nucleotide substitutions, one insertion and one deletion).
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     
MYL2 NM_000432.3 ./. 03 c.132T>C - p.Ile44Ile