Variant #0000262870 (NC_000023.10:g.153175521G>A, ARHGAP4(NM_001666.4):c.2175C>T)

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.153175521G>A
DNA change (hg38) g.153910067G>A
Published as ARHGAP4(NM_001164741.1):c.2295C>T (p.S765=)
ISCN -
DB-ID ARHGAP4_000028
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
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.*3339G>A r.(=) p.(=)
ARHGAP4 NM_001666.4 -?/. - c.2175C>T r.(?) p.(Ser725=)