Variant #0000441298 (NC_000003.11:g.189582119C>T, NM_003722.4:c.678C>T (TP63))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.189582119C>T
DNA change (hg38) g.189864330C>T
Published as -
ISCN -
DB-ID TP63_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs61732782
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00026 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 11:20:42 +01:00 (CET)
Date last edited 2024-10-10 22:41:50 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TP63 NM_001114979.1 ./. - c.678C>T r.(=) p.(=) -
TP63 NM_003722.4 -/- 5 c.678C>T r.(?) p.= -


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