Variant #0001015999 (NC_000023.10:g.153196275A>G, NM_001666.4:c.-4619T>C (ARHGAP4))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153196275A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARHGAP4_000131
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP4 NM_001666.4 +?/. - c.-4619T>C r.(?) p.(=)
RENBP NM_002910.5 +?/. - c.*4464T>C r.(=) p.(=)
NAA10 NM_003491.3 +?/. - c.412T>C r.(?) p.(Tyr138His)


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