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
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