Variant #0000719698 (NC_000004.11:g.111542322G>A, NM_153426.2:c.388C>T (PITX2))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.111542322G>A
DNA change (hg38) -
Published as PITX2(NM_001204397.1):c.388C>T (p.R130W)
ISCN -
DB-ID PITX2_000055
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITX2 NM_000325.5 +?/. - c.409C>T r.(?) p.(Arg137Trp)
PITX2 NM_153426.2 +?/. - c.388C>T r.(?) p.(Arg130Trp)


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