Variant #0000340105 (NC_000020.10:g.45194904C>G, NM_033550.3:c.*120488G>C (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.45194904C>G
DNA change (hg38) g.46566265C>G
Published as -
ISCN -
DB-ID SLC13A3_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) 0.14315 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 17:59:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC13A3 NM_001011554.2 -/. - c.1317G>C r.(?) p.(Ala439=)
TP53RK NM_033550.3 -/. - c.*120488G>C r.(=) p.(=)


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