Variant #0000126771 (NC_000011.9:g.22272339T>G, NM_213599.2:c.1066T>G (ANO5))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.22272339T>G
DNA change (hg38) g.22250793T>G
Published as -
ISCN -
DB-ID ANO5_000002 See all 3 reported entries
Variant remarks cDNA expression cloning COS-7 cells shows decreased cell adhesion, changed cell morphology (round)
Reference PubMed: Tsutsumi 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-02-14 22:37:07 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO5 NM_213599.2 +?/. 11 c.1066T>G r.1066u>g p.Cys356Gly


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.