Variant #0000000036 (NC_000011.9:g.76873185A>C, MYO7A(NM_000260.3):c.1363A>C)

Individual ID 00000049
Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.76873185A>C
Reference -
DB-ID MYO7A_000002
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
MYO7A NM_000260.3 +/+ - c.1363A>C r.(?) p.(Asn455His) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000049 DNA SEQ-NG MYO7A 1 variome.ir