Variant #0000698280 (NC_000011.9:g.76885835C>T, NM_000260.3:c.1969C>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.76885835C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO7A_000410 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs878853236
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 2020-10-22 18:03:01 +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.1969C>T r.(?) p.(Arg657Trp) -


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