Variant #0000568787 (NC_000019.9:g.7531856C>T, NM_001130955.1:c.2393C>T (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.7531856C>T
DNA change (hg38) g.7466970C>T
Published as ARHGEF18(NM_001130955.2):c.2231C>T (p.S744L), ARHGEF18(NM_001367823.1):c.2957C>T (p.S986L)
ISCN -
DB-ID ARHGEF18_000019 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) 0.00065 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 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 -?/. - c.2393C>T r.(?) p.(Ser798Leu)
ARHGEF18 NM_015318.3 -?/. - c.1919C>T r.(?) p.(Ser640Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.