Variant #0000950763 (NC_000016.9:g.88876886C>T, NM_000485.2:c.266G>A (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.88876886C>T
DNA change (hg38) -
Published as APRT(NM_000485.3):c.266G>A (p.R89Q)
ISCN -
DB-ID APRT_000016
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) 0.00089 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.266G>A r.(?) p.(Arg89Gln)
GALNS NM_000512.4 -?/. - c.*3961G>A r.(=) p.(=)
CDT1 NM_030928.3 -?/. - c.*2200C>T r.(=) p.(=)


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