Variant #0000441290 (NC_000003.11:g.189586438G>A, NM_003722.4:c.1062G>A (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.189586438G>A
DNA change (hg38) g.189868649G>A
Published as -
ISCN -
DB-ID TP63_000014
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34841666
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00058 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 11:31:40 +01:00 (CET)
Date last edited 2018-12-23 11:56:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TP63 NM_001114979.1 ./. - c.1062G>A r.(=) p.(=) -
TP63 NM_003722.4 -/- 8 c.1062G>A r.(?) p.(=) -


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