Variant #0000018016 (NC_000005.9:g.13900321G>T, NM_001369.2:c.2253C>A (DNAH5))
| Chromosome |
5 |
| Allele |
Parent #2 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13900321G>T |
| DNA change (hg38) |
g.13900212G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DNAH5_000002 See all 4 reported entries |
| Variant remarks |
variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
1 |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00988 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-05-08 23:53:32 +02:00 (CEST) |
| Date last edited |
2013-05-31 18:48:34 +02:00 (CEST) |

Variant on transcripts
Screenings
|