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 International |
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) |

Variant on transcripts
|