Variant #0000441286 (NC_000003.11:g.189526354T>A, NC_000003.11(NM_003722.4):c.579+39T>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.189526354T>A
DNA change (hg38) g.189808565T>A
Published as -
ISCN -
DB-ID TP63_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34429985
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00051 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 11:18:46 +01:00 (CET)
Date last edited 2018-12-23 11:56:13 +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.579+39T>A r.(=) p.(=) -
TP63 NM_003722.4 -/- 4i c.579+39T>A r.(?) p.(=) -


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