Variant #0000728589 (NC_000023.10:g.153195656C>T, NM_001666.4:c.-4000G>A (ARHGAP4))

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.153195656C>T
DNA change (hg38) -
Published as NAA10(NM_003491.3):c.492G>A (p.L164=)
ISCN -
DB-ID ARHGAP4_000109
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP4 NM_001666.4 -?/. - c.-4000G>A r.(?) p.(=)
NAA10 NM_003491.3 -?/. - c.492G>A r.(?) p.(Leu164=)


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