Variant #0000809108 (NC_000019.9:g.7531803G>T, NC_000019.9(NM_001130955.1):c.2341-1G>T (ARHGEF18))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7531803G>T
DNA change (hg38) -
Published as ARHGEF18(NM_001367823.1):c.2905-1G>T
ISCN -
DB-ID ARHGEF18_000055
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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 +?/. - c.2341-1G>T r.spl? p.?
ARHGEF18 NM_015318.3 +?/. - c.1867-1G>T r.spl? p.?


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