Variant #0000568782 (NC_000019.9:g.7524887G>A, NC_000019.9(NM_001130955.1):c.1888+7G>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.7524887G>A
DNA change (hg38) g.7460001G>A
Published as ARHGEF18(NM_001130955.2):c.1726+7G>A
ISCN -
DB-ID ARHGEF18_000014
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) 0.00035 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 2020-08-06 14:59:34 +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.1888+7G>A r.(=) p.(=)
ARHGEF18 NM_015318.3 -?/. - c.1414+7G>A r.(=) p.(=)


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