Variant #0000866352 (NC_000019.9:g.7532258G>C, NM_001130955.1:c.2604G>C (ARHGEF18))
| Chromosome |
19 |
| 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.7532258G>C |
| DNA change (hg38) |
- |
| Published as |
ARHGEF18(NM_001130955.2):c.2442G>C (p.L814=), ARHGEF18(NM_001367823.1):c.3168G>C (p.L1056=) |
| ISCN |
- |
| DB-ID |
ARHGEF18_000021 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) |
0.00035 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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