Variant #0000524593 (NC_000005.9:g.140953592_140953597dup, NM_005219.4:c.1848_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.140953592_140953597dup |
DNA change (hg38) |
g.141574025_141574030dup |
Published as |
DIAPH1(NM_005219.4):c.1848_1853dupTCCTCC (p.P619_P620dup), DIAPH1(NM_005219.5):c.1842_1847dupTCCTCC (p.P619_P620dup), DIAPH1(NM_005219.5):c.1848_18... |
ISCN |
- |
DB-ID |
DIAPH1_000057 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
|