ClinVar Miner

List of variants in gene TP63 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003722.5(TP63):c.1350-23T>C rs1345186 0.74615
NM_003722.5(TP63):c.1130-22A>G rs6789961 0.32652
NM_003722.5(TP63):c.1349+41G>A rs9840360 0.25021
NM_003722.5(TP63):c.766+42G>A rs2276792 0.19026
NM_003722.5(TP63):c.766+34T>G rs17514215 0.11812
NM_003722.5(TP63):c.*45C>T rs34057105 0.05395
NM_003722.5(TP63):c.191+24T>C rs34875865 0.03673
NM_003722.5(TP63):c.1652+46G>A rs35558939 0.03124
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049 0.01380
NM_003722.5(TP63):c.1652+14A>C rs150685395 0.01158
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr) rs148076109 0.00295
NM_003722.5(TP63):c.399C>T (p.Pro133=) rs145730343 0.00196
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552 0.00082
NM_003722.5(TP63):c.2034G>A (p.Glu678=) rs140508531 0.00021
NM_003722.5(TP63):c.2021G>A (p.Arg674His) rs34713855 0.00006
NM_003722.5(TP63):c.1349+40G>C rs9840359
NM_003722.5(TP63):c.1350-34T>G rs1554131
NM_003722.5(TP63):c.192-9_192-8del rs794727498
NM_003722.5(TP63):c.324+7G>A rs930341004
NM_003722.5(TP63):c.587C>G (p.Thr196Ser)
NM_003722.5(TP63):c.876A>G (p.Pro292=) rs886038535

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.