Variant #0000855857 (NC_000020.10:g.45315750G>A, NM_033550.3:c.404C>T (TP53RK))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45315750G>A
DNA change (hg38) -
Published as TP53RK(NM_033550.4):c.404C>T (p.T135I)
ISCN -
DB-ID SLC13A3_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) 0.00184 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 2022-05-09 15:47:41 +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     
SLC13A3 NM_001011554.2 -/. - c.-2843C>T r.(?) p.(=)
TP53RK NM_033550.3 -/. - c.404C>T r.(?) p.(Thr135Ile)


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