Variant #0000324998 (NC_000016.9:g.88876121G>A, NM_000485.2:c.528C>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.88876121G>A
DNA change (hg38) g.88809713G>A
Published as APRT(NM_000485.2):c.528C>T (p.(=))
ISCN -
DB-ID APRT_000001
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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-10 15:55:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APRT NM_000485.2 ?/. - c.528C>T r.(?) p.(Leu176=)
GALNS NM_000512.4 ?/. - c.*4726C>T r.(=) p.(=)
CDT1 NM_030928.3 ?/. - c.*1435G>A r.(=) p.(=)


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