Variant #0000866349 (NC_000019.9:g.7518524G>A, NM_001130955.1:c.1463G>A (ARHGEF18))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7518524G>A
DNA change (hg38) -
Published as ARHGEF18(NM_001367823.1):c.2027G>A (p.R676H)
ISCN -
DB-ID ARHGEF18_000061
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.1463G>A r.(?) p.(Arg488His)
ARHGEF18 NM_015318.3 ?/. - c.989G>A r.(?) p.(Arg330His)


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