Variant #0001033860 (NC_000003.11:g.189607126C>T, NC_000003.11(NM_003722.4):c.1508-3C>T (TP63))

Chromosome 3
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.189607126C>T
DNA change (hg38) -
Published as TP63(NM_003722.5):c.1508-3C>T
ISCN -
DB-ID TP63_000125
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     

P-domain     
TP63 NM_001114979.1 -?/. - c.*9159C>T r.(=) p.(=) -
TP63 NM_003722.4 -?/. - c.1508-3C>T r.spl? p.? -


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