Variant #0000759743 (NC_000011.9:g.76901152C>T, NM_000260.3:c.3718C>T (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.76901152C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO7A_000152 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs371374104
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-03-15 16:01:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +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.3718C>T r.(?) p.(Arg1240Trp) -


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