Variant #0000559720 (NC_000016.9:g.88871972G>A, NM_000485.2:c.*4134C>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.88871972G>A
DNA change (hg38) g.88805564G>A
Published as CDT1(NM_030928.3):c.613G>A (p.(Gly205Ser))
ISCN -
DB-ID CDT1_000002 See all 3 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) 0.00235 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.*4134C>T r.(=) p.(=)
CDT1 NM_030928.3 -?/. - c.613G>A r.(?) p.(Gly205Ser)


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