Variant #0000728588 (NC_000023.10:g.153195571C>G, ARHGAP4(NM_001666.4):c.-3915G>C)

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.153195571C>G
DNA change (hg38) -
Published as NAA10(NM_003491.3):c.577G>C (p.A193P)
ISCN -
DB-ID ARHGAP4_000108
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP4 NM_001666.4 -?/. - c.-3915G>C r.(?) p.(=)
NAA10 NM_003491.3 -?/. - c.577G>C r.(?) p.(Ala193Pro)