Variant #0001064409 (NC_000005.9:g.134369552C>A, NM_002653.4:c.20G>T (PITX1))

Chromosome 5
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.134369552C>A
DNA change (hg38) -
Published as PITX1(NM_002653.5):c.20G>T (p.(Gly7Val))
ISCN -
DB-ID chr5_007856
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITX1 NM_002653.4 ?/. - c.20G>T r.(?) p.(Gly7Val)
H2AFY NM_004893.2 ?/. - c.*301114G>T r.(=) p.(=)


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