Variant #0000336123 (NC_000023.10:g.153196209C>T, ARHGAP4(NM_001666.4):c.-4553G>A)
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.153196209C>T |
DNA change (hg38) |
g.153930756C>T |
Published as |
NAA10(NM_001256119.1):c.426+7G>A (p.(=)), NAA10(NM_003491.3):c.471+7G>A |
ISCN |
- |
DB-ID |
NAA10_000012 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 |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |

Variant on transcripts
|
|