Variant #0000617935 (NC_000019.9:g.7532417G>T, NM_001130955.1:c.2763G>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.7532417G>T
DNA change (hg38) g.7467531G>T
Published as ARHGEF18(NM_001130955.2):c.2601G>T (p.L867=)
ISCN -
DB-ID ARHGEF18_000027
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 -?/. - c.2763G>T r.(?) p.(Leu921=)
ARHGEF18 NM_015318.3 -?/. - c.2289G>T r.(?) p.(Leu763=)


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