Variant #0000296985 (NC_000004.11:g.111539489C>T, NM_153426.2:c.746G>A (PITX2))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111539489C>T
DNA change (hg38) g.110618333C>T
Published as PITX2(NM_001204397.2):c.746G>A (p.S249N)
ISCN -
DB-ID PITX2_000033
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITX2 NM_000325.5 ?/. - c.767G>A r.(?) p.(Ser256Asn)
PITX2 NM_153426.2 ?/. - c.746G>A r.(?) p.(Ser249Asn)


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