Variant #0000534422 (NC_000008.10:g.1833804C>T, NM_014629.2:c.1113C>T (ARHGEF10))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1833804C>T |
DNA change (hg38) |
g.1885638C>T |
Published as |
ARHGEF10(NM_001308153.2):c.1188C>T (p.F396=) |
ISCN |
- |
DB-ID |
ARHGEF10_000057 |
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) |
0.01141 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-06-23 15:31:24 +02:00 (CEST) |

Variant on transcripts
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