Variant #0000866943 (NC_000023.10:g.101971255C>T, ARMCX5(NM_022838.3):c.*112509C>T)
Chromosome |
X |
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.101971255C>T |
DNA change (hg38) |
- |
Published as |
ARMCX5-GPRASP2(NM_001199818.1):c.1458C>T (p.S486=), GPRASP2(NM_001184874.2):c.1458C>T (p.S486=) |
ISCN |
- |
DB-ID |
ARMCX5_000036 |
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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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