Variant #0000058633 (NC_000004.11:g.111542442T>C, NM_153426.2:c.268A>G (PITX2))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.111542442T>C
DNA change (hg38) g.110621286T>C
Published as NM_000325.5:c.289A>G (T97A)
ISCN -
DB-ID PITX2_000026 See all 2 reported entries
Variant remarks T97A expression cloning CHO cells reduced activation (0.2) atrial natriuretic factor promoter
Reference PubMed: Zuo 2013, Journal: Zuo 2013
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 2015-02-20 21:11:44 +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     
PITX2 NM_000325.5 ?/. - c.289A>G r.(?) p.(Thr97Ala)
PITX2 NM_153426.2 ?/. 5 c.268A>G r.(?) p.(Thr90Ala)


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