Variant #0000692200 (NC_000016.9:g.88873815G>A, NM_000485.2:c.*2291C>T (APRT))

Chromosome 16
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.88873815G>A
DNA change (hg38) -
Published as CDT1(NM_030928.3):c.1402G>A (p.E468K), CDT1(NM_030928.4):c.1402G>A (p.(Glu468Lys))
ISCN -
DB-ID APRT_000069 See all 2 reported entries
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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APRT NM_000485.2 ?/. - c.*2291C>T r.(=) p.(=)
CDT1 NM_030928.3 ?/. - c.1402G>A r.(?) p.(Glu468Lys)


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