Variant #0000721899 (NC_000008.10:g.1844621C>T, NC_000008.10(NM_014629.2):c.1557+6C>T (ARHGEF10))
Chromosome |
8 |
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.1844621C>T |
DNA change (hg38) |
- |
Published as |
ARHGEF10(NM_001308153.1):c.1632+6C>T, ARHGEF10(NM_001308153.2):c.1632+6C>T |
ISCN |
- |
DB-ID |
ARHGEF10_000089 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) |
0.00013 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
|