Variant #0000568775 (NC_000019.9:g.7505367G>A, NM_001130955.1:c.541G>A (ARHGEF18))

Chromosome 19
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.7505367G>A
DNA change (hg38) g.7440481G>A
Published as ARHGEF18(NM_001130955.2):c.379G>A (p.G127R), ARHGEF18(NM_001367823.1):c.1105G>A (p.G369R)
ISCN -
DB-ID ARHGEF18_000007 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) 0.00127 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 -?/. - c.541G>A r.(?) p.(Gly181Arg)
ARHGEF18 NM_015318.3 -?/. - c.67G>A r.(?) p.(Gly23Arg)


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