Variant #0000982179 (NC_000016.9:g.88871230C>T, NM_000485.2:c.*4876G>A (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.88871230C>T
DNA change (hg38) -
Published as CDT1(NM_030928.4):c.412C>T (p.(Arg138Trp))
ISCN -
DB-ID APRT_000077
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) 0.00021 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APRT NM_000485.2 ?/. - c.*4876G>A r.(=) p.(=)
CDT1 NM_030928.3 ?/. - c.412C>T r.(?) p.(Arg138Trp)


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