Variant #0000011505 (NC_000012.11:-, MYL2(NM_000432.3):c.37G>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type human cosmid
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MYL2_00003 See all 4 reported entries
Frequency -
Variant remarks The amino acid that is mutated, as well as the flanking sequence, shows strong evolutionary conservation. The individual with the Ala13Thr mutation was strikingly similar to that seen in patients with ELC mutations in that is showed the pronounced mid cavity obstruction.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 ./. 02 c.37G>A - p.Ala13Thr