Variant #0000855732 (NC_000019.9:g.7447761T>C, NM_001130955.1:c.-57066T>C (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.7447761T>C
DNA change (hg38) -
Published as ARHGEF18(NM_001367823.1):c.806T>C (p.V269A)
ISCN -
DB-ID ARHGEF18_000059 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) 0.00068 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 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF18 NM_001130955.1 ?/. - c.-57066T>C r.(?) p.(=)
ARHGEF18 NM_015318.3 ?/. - c.-12444T>C r.(?) p.(=)


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