Variant #0000966594 (NC_000011.9:g.76841670G>A, NM_000260.3:c.-11G>A (MYO7A))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76841670G>A
DNA change (hg38) -
Published as MYO7A(NM_000260.4):c.-11G>A
ISCN -
DB-ID CAPN5_000076
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO7A NM_000260.3 -?/. - c.-11G>A r.(?) p.(=) -
CAPN5 NM_004055.4 -?/. - c.*6754G>A r.(=) p.(=) -
OMP NM_006189.1 -?/. - c.*27293G>A r.(=) p.(=) -


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