Variant #0000574459 (NC_000023.10:g.153196242G>A, ARHGAP4(NM_001666.4):c.-4586C>T)

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.153196242G>A
DNA change (hg38) g.153930789G>A
Published as -
ISCN -
DB-ID ARHGAP4_000079
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP4 NM_001666.4 ?/. - c.-4586C>T r.(?) p.(=)
RENBP NM_002910.5 ?/. - c.*4497C>T r.(=) p.(=)
NAA10 NM_003491.3 ?/. - c.445C>T r.(?) p.(Arg149Trp)