ClinVar Miner

List of variants in gene TP53 reported as benign for Cushing syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578
NM_000546.6(TP53):c.*328G>A
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522
NM_000546.6(TP53):c.639A>G (p.Arg213=) rs1800372
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519
NM_000546.6(TP53):c.903A>G (p.Pro301=) rs72661120
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_001126112.2(TP53):c.*1070C>T rs114831472
NM_001126112.2(TP53):c.*1175A>C rs78378222
NM_001126112.2(TP53):c.*205G>A rs16956880
NM_001126112.2(TP53):c.*485G>A rs4968187
NM_001126112.2(TP53):c.*613C>A rs17879353
NM_001126112.2(TP53):c.*773C>T rs200378797
NM_001126112.2(TP53):c.*826G>A rs17884306
NM_001126112.2(TP53):c.108G>A (p.Pro36=) rs1800370
NM_001126112.2(TP53):c.141G>A (p.Pro47=) rs201741778
NM_001126112.2(TP53):c.217G>A (p.Val73Met) rs587782423
NM_001126112.2(TP53):c.560-8G>C rs373797299
NM_001126112.2(TP53):c.63C>T (p.Asp21=) rs1800369
NM_001126112.2(TP53):c.673-36G>C rs17880604
NM_001126112.2(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_001126112.2(TP53):c.97-6C>T rs35117667
NM_001126112.2(TP53):c.993+12T>C rs1800899

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