Variant #0000568793 (NC_000019.9:g.7533891G>A, NM_001130955.1:c.3097G>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.7533891G>A
DNA change (hg38) g.7469005G>A
Published as ARHGEF18(NM_001367823.1):c.3661G>A (p.A1221T), ARHGEF18(NM_015318.3):c.2623G>A (p.A875T)
ISCN -
DB-ID ARHGEF18_000025 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) 0.00318 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 -?/. - c.3097G>A r.(?) p.(Ala1033Thr)
ARHGEF18 NM_015318.3 -?/. - c.2623G>A r.(?) p.(Ala875Thr)


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