Variant #0000648874 (NC_000014.8:g.24563620C>T, PCK2(NM_001018073.1):c.6C>T)

Individual ID 00291017
Chromosome 14
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24563620C>T
DNA change (hg38) g.24094411C>T
Published as -
ISCN -
DB-ID PCK2_000003
Variant remarks 50 heterozygous, no homozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs77298044
Origin Germline
Segregation -
Frequency 50/2782 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02034 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCK2 NM_001018073.1 -/. - c.6C>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000292185 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq