Variant #0000807696 (NC_000016.9:g.88871291G>A, NM_000485.2:c.*4815C>T (APRT))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88871291G>A
DNA change (hg38) -
Published as CDT1(NM_030928.3):c.473G>A (p.R158H, p.(Arg158His))
ISCN -
DB-ID CDT1_000008 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) 0.00019 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 2021-09-17 14:40:49 +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.*4815C>T r.(=) p.(=)
CDT1 NM_030928.3 -?/. - c.473G>A r.(?) p.(Arg158His)


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