Variant #0000921501 (NC_000011.9:g.76867967_76867972del, NM_000260.3:c.652_657del (MYO7A))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76867967_76867972del
DNA change (hg38) g.77156921_77156926del
Published as -
ISCN -
DB-ID MYO7A_000128 See all 3 reported entries
Variant remarks PM2_P, PM3_P, PM4_M, PP1_P, PP4_P, following ClinGen GN005
Reference -
ClinVar ID -
dbSNP ID rs1555062984
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-03-17 17:31:01 +01:00 (CET)
Date last edited 2023-03-17 17:33:02 +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 +?/+? 07 c.652_657del r.(?) p.(Asp218_Ile219del) Myosin motor (65 - 741)


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