Variant #0000866352 (NC_000019.9:g.7532258G>C, NM_001130955.1:c.2604G>C (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.7532258G>C
DNA change (hg38) -
Published as ARHGEF18(NM_001130955.2):c.2442G>C (p.L814=), ARHGEF18(NM_001367823.1):c.3168G>C (p.L1056=)
ISCN -
DB-ID ARHGEF18_000021 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) 0.00035 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 -?/. - c.2604G>C r.(?) p.(Leu868=)
ARHGEF18 NM_015318.3 -?/. - c.2130G>C r.(?) p.(Leu710=)


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