Variant #0000253109 (NC_000005.9:g.73072504A>C, NM_001080479.2:c.823A>C (ARHGEF28))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73072504A>C
DNA change (hg38) g.73776679A>C
Published as ARHGEF28(NM_001080479.2):c.823A>C (p.R275=), ARHGEF28(NM_001080479.3):c.823A>C (p.R275=)
ISCN -
DB-ID ARHGEF28_000004 See all 5 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) 0.03283 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGEF28 NM_001080479.2 -/. - c.823A>C r.(?) p.(Arg275=)


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