Variant #0001051620 (NC_000003.11:g.196018226A>C, NM_005017.2:c.-3815T>G (PCYT1A))

Chromosome 3
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.196018226A>C
DNA change (hg38) -
Published as TCTEX1D2(NM_152773.5):c.401T>G (p.(Val134Gly))
ISCN -
DB-ID TCTEX1D2_000007
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCYT1A NM_005017.2 ?/. - c.-3815T>G r.(?) p.(=)
TCTEX1D2 NM_152773.4 ?/. - c.401T>G r.(?) p.(Val134Gly)


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