Variant #0000163168 (NC_000001.10:g.94654810A>G, NM_004815.3:c.1538T>C (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.94654810A>G
DNA change (hg38) g.94189254A>G
Published as Ile513Thr
ISCN -
DB-ID ARHGAP29_000002 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) 0.00054 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 -?/. 14 c.1538T>C r.(?) p.Ile513Thr


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