Variant #0000693443 (NC_000023.10:g.153175189A>G, ARHGAP4(NM_001666.4):c.2414+6T>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.153175189A>G
DNA change (hg38) -
Published as ARHGAP4(NM_001164741.1):c.2534+6T>C, ARHGAP4(NM_001164741.2):c.2534+6T>C
ISCN -
DB-ID ARHGAP4_000026 See all 2 reported entries
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) 0.00041 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.*3007A>G r.(=) p.(=)
ARHGAP4 NM_001666.4 -?/. - c.2414+6T>C r.(=) p.(=)