Variant #0000569781 (NC_000020.10:g.43995543C>T, NM_014477.2:c.*7004G>A (TP53TG5))

Chromosome 20
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.43995543C>T
DNA change (hg38) g.45366903C>T
Published as SYS1(NM_001197129.1):c.259C>T (p.R87*)
ISCN -
DB-ID DBNDD2_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53TG5 NM_014477.2 ?/. - c.*7004G>A r.(=) p.(=)
DBNDD2 NM_018478.3 ?/. - c.-39549C>T r.(?) p.(=)
SYS1 NM_033542.3 ?/. - c.259C>T r.(?) p.(Arg87Ter)
SYS1-DBNDD2 NR_003189.2 ?/. - n.380+1217C>T r.(?) -


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