Variant #0000545827 (NC_000011.9:g.76900431C>A, NM_000260.3:c.3546C>A (MYO7A))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76900431C>A
DNA change (hg38) g.77189386C>A
Published as MYO7A(NM_000260.3):c.3546C>A (p.N1182K), MYO7A(NM_000260.4):c.3546C>A (p.N1182K)
ISCN -
DB-ID MYO7A_000581 See all 10 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-06 12:43:26 +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.3546C>A r.(?) p.(Asn1182Lys) -


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