Variant #0000814678 (NC_000011.9:g.76892635G>T, NM_000260.3:c.2904G>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.76892635G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO7A_000205 See all 18 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs111033233
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-10-13 10:38:01 +02:00 (CEST)
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.2904G>T r.(?) p.(Glu968Asp) -


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