Variant #0000621494 (NC_000005.9:g.140953310G>C, NM_005219.4:c.2107C>G (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.140953310G>C |
DNA change (hg38) |
g.141573743G>C |
Published as |
DIAPH1(NM_001314007.1):c.2107C>G (p.P703A) |
ISCN |
- |
DB-ID |
DIAPH1_000024 See all 2 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) |
0.00016 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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