Variant #0000272603 (NC_000011.9:g.76834880G>A, NM_000260.3:c.-4702G>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.76834880G>A
DNA change (hg38) g.77123834G>A
Published as CAPN5(NM_004055.4):c.1887G>A (p.V629=)
ISCN -
DB-ID CAPN5_000014
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 10:40:19 +02:00 (CEST)
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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.-4702G>A r.(?) p.(=) -
CAPN5 NM_004055.4 -?/. - c.1887G>A r.(?) p.(Val629=) -
OMP NM_006189.1 -?/. - c.*20503G>A r.(=) p.(=) -


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