Variant #0000617937 (NC_000019.9:g.7534862G>A, NM_001130955.1:c.3296G>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.7534862G>A
DNA change (hg38) g.7469976G>A
Published as ARHGEF18(NM_001130955.2):c.3134G>A (p.R1045H)
ISCN -
DB-ID ARHGEF18_000029
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) 1.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 ?/. - c.3296G>A r.(?) p.(Arg1099His)
ARHGEF18 NM_015318.3 ?/. - c.2822G>A r.(?) p.(Arg941His)


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