Variant #0000850483 (NC_000004.11:g.111553640G>A, NC_000004.11(NM_153426.2):c.47-4C>T (PITX2))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111553640G>A
DNA change (hg38) -
Published as PITX2(NM_001204397.1):c.47-4C>T (p.?)
ISCN -
DB-ID PITX2_000070
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:40:45 +02:00 (CEST)
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.-10024C>T r.(?) p.(=)
PITX2 NM_153426.2 -?/. - c.47-4C>T r.spl? p.?


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