Variant #0000518735 (NC_000003.11:g.189586404G>A, NM_003722.4:c.1028G>A (TP63))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.189586404G>A
DNA change (hg38) g.189868615G>A
Published as TP63(NM_003722.5):c.1028G>A (p.R343Q)
ISCN -
DB-ID TP63_000090 See all 2 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TP63 NM_001114979.1 +/. - c.1028G>A r.(?) p.(Arg343Gln) -
TP63 NM_003722.4 +/. - c.1028G>A r.(?) p.(Arg343Gln) -


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