Variant #0001033875 (NC_000003.11:g.195959364G>T, NM_005017.2:c.*6195C>A (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.195959364G>T
DNA change (hg38) -
Published as SLC51A(NM_152672.6):c.855G>T (p.(Ser285=))
ISCN -
DB-ID PCYT1A_000039
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) 2.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
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.*6195C>A r.(=) p.(=)
SLC51A NM_152672.5 ?/. - c.855G>T r.(?) p.(=)


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