Variant #0000613725 (NC_000011.9:g.76834781C>A, NM_000260.3:c.-4801C>A (MYO7A))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76834781C>A
DNA change (hg38) g.77123735C>A
Published as CAPN5(NM_004055.4):c.1788C>A (p.H596Q)
ISCN -
DB-ID CAPN5_000039
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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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.-4801C>A r.(?) p.(=) -
CAPN5 NM_004055.4 ?/. - c.1788C>A r.(?) p.(His596Gln) -
OMP NM_006189.1 ?/. - c.*20404C>A r.(=) p.(=) -


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