Variant #0000574424 (NC_000023.10:g.153171445T>C, ARHGAP4(NM_001666.4):c.*1738A>G)

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.153171445T>C
DNA change (hg38) g.153905991T>C
Published as AVPR2(NM_001146151.2):c.485T>C (p.V162A)
ISCN -
DB-ID ARHGAP4_000051
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) 6.0E-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     
AVPR2 NM_000054.4 -?/. - c.485T>C r.(?) p.(Val162Ala)
ARHGAP4 NM_001666.4 -?/. - c.*1738A>G r.(=) p.(=)