ClinVar Miner

List of variants in gene TP63 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 3q28(chr3:189364424-189379493)x1
GRCh37/hg19 3q28(chr3:189383139-189397549)x3
NM_003722.4(TP63):c.*2789A>G rs11708746
NM_003722.5(TP63):c.*1844dup rs146332971
NM_003722.5(TP63):c.*2345C>T rs35592567
NM_003722.5(TP63):c.*2544del rs201395656
NM_003722.5(TP63):c.*435C>T rs78233713
NM_003722.5(TP63):c.*45C>T rs34057105
NM_003722.5(TP63):c.*541G>A rs73199799
NM_003722.5(TP63):c.*638C>G rs6444406
NM_003722.5(TP63):c.1130-22A>G rs6789961
NM_003722.5(TP63):c.1349+40G>C rs9840359
NM_003722.5(TP63):c.1349+41G>A rs9840360
NM_003722.5(TP63):c.1350-23T>C rs1345186
NM_003722.5(TP63):c.1350-34T>G rs1554131
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552
NM_003722.5(TP63):c.1788G>A (p.Ala596=)
NM_003722.5(TP63):c.191+24T>C rs34875865
NM_003722.5(TP63):c.192-9_192-8del rs794727498
NM_003722.5(TP63):c.366G>A (p.Gln122=)
NM_003722.5(TP63):c.399C>T (p.Pro133=) rs145730343
NM_003722.5(TP63):c.673A>G (p.Ile225Val)
NM_003722.5(TP63):c.766+34T>G rs17514215
NM_003722.5(TP63):c.766+42G>A rs2276792
NM_003722.5(TP63):c.84T>G (p.His28Gln)
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.