Variant #0001019337 (NC_000005.9:g.140953589_140953597dup, NM_005219.4:c.1845_1853dup (DIAPH1))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.140953589_140953597dup |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
DIAPH1_000110 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
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 International |
Created by |
MobiDetails |
Date created |
2024-12-20 15:03:01 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|