Variant #0000866509 (NC_000020.10:g.44003909C>T, NM_014477.2:c.538G>A (TP53TG5))

Chromosome 20
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.44003909C>T
DNA change (hg38) -
Published as TP53TG5(NM_014477.3):c.538G>A (p.E180K)
ISCN -
DB-ID DBNDD2_000002
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) 2.0E-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 2022-05-09 16:01:56 +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     
TP53TG5 NM_014477.2 -?/. - c.538G>A r.(?) p.(Glu180Lys)
DBNDD2 NM_018478.3 -?/. - c.-31183C>T r.(?) p.(=)
SYS1 NM_033542.3 -?/. - c.*8154C>T r.(=) p.(=)
SYS1-DBNDD2 NR_003189.2 -?/. - n.380+9583C>T r.(?) -


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