Variant #0000518738 (NC_000003.11:g.189590644A>G, NC_000003.11(NM_003722.4):c.1213-4A>G (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.189590644A>G
DNA change (hg38) g.189872855A>G
Published as TP63(NM_001114978.1):c.1213-4A>G (p.?)
ISCN -
DB-ID TP63_000092
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 09:39:20 +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.1213-4A>G r.spl? p.? -
TP63 NM_003722.4 -?/. - c.1213-4A>G r.spl? p.? -


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