Variant #0000163169 (NC_000001.10:g.94645368C>T, NM_004815.3:c.2393G>A (ARHGAP29))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.94645368C>T
DNA change (hg38) g.94179812C>T
Published as Arg798Gln
ISCN -
DB-ID ARHGAP29_000003 See all 2 reported entries
Variant remarks cDNA expression cloning in iNHK cells (scratch assay) revealed normal migration
Reference PubMed: Liu 2016, Journal: Liu 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00179 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-02-17 17:34:09 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP29 NM_004815.3 -?/. 20 c.2393G>A r.(?) p.Arg798Gln


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