ClinVar Miner

List of variants in gene TP53 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.173C>G (p.Pro58Arg) rs144386518 0.00027
NM_000546.6(TP53):c.1079G>C (p.Gly360Ala) rs35993958 0.00019
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_000546.6(TP53):c.618G>A (p.Leu206=) rs142813240 0.00007
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys) rs17882252 0.00006
NM_000546.6(TP53):c.*6T>A rs369567704 0.00005
NM_000546.6(TP53):c.102C>G (p.Pro34=) rs11575998 0.00004
NM_000546.6(TP53):c.255T>C (p.Pro85=) rs775515332 0.00004
NM_000546.6(TP53):c.180A>C (p.Pro60=) rs749289195 0.00003
NM_000546.6(TP53):c.246G>A (p.Pro82=) rs372397095 0.00003
NM_000546.6(TP53):c.18A>C (p.Ser6=) rs573130482 0.00002
NM_000546.6(TP53):c.234A>G (p.Ala78=) rs375099397 0.00002
NM_000546.6(TP53):c.249G>A (p.Ala83=) rs55754907 0.00002
NM_000546.6(TP53):c.582T>C (p.Leu194=) rs370216745 0.00002
NM_000546.6(TP53):c.782+10C>T rs200277687 0.00002
NM_000546.6(TP53):c.1131C>T (p.Thr377=) rs1456836660 0.00001
NM_000546.6(TP53):c.123T>C (p.Asp41=) rs369129220 0.00001
NM_000546.6(TP53):c.12G>A (p.Pro4=) rs876658274 0.00001
NM_000546.6(TP53):c.145G>A (p.Asp49Asn) rs587780728 0.00001
NM_000546.6(TP53):c.270C>T (p.Ser90=) rs863224370 0.00001
NM_000546.6(TP53):c.354A>T (p.Thr118=) rs751978853 0.00001
NM_000546.6(TP53):c.45T>C (p.Ser15=) rs766765429 0.00001
NM_000546.6(TP53):c.468C>T (p.Arg156=) rs761222871 0.00001
NM_000546.6(TP53):c.469G>A (p.Val157Ile) rs121912654 0.00001
NM_000546.6(TP53):c.54A>G (p.Thr18=) rs876659984 0.00001
NM_000546.6(TP53):c.566C>T (p.Ala189Val) rs121912665 0.00001
NM_000546.6(TP53):c.606T>C (p.Arg202=) rs1392931620 0.00001
NM_000546.6(TP53):c.66A>G (p.Leu22=) rs748527030 0.00001
NM_000546.6(TP53):c.855G>A (p.Glu285=) rs1487868349 0.00001
NM_000546.6(TP53):c.867C>T (p.Leu289=) rs778138282 0.00001
NM_000546.6(TP53):c.877G>T (p.Gly293Trp) rs587780076 0.00001
NM_000546.6(TP53):c.891C>T (p.His297=) rs750578863 0.00001
NM_000546.6(TP53):c.1011C>G (p.Arg337=) rs1218459955
NM_000546.6(TP53):c.1041C>G (p.Ala347=) rs1450229137
NM_000546.6(TP53):c.1079G>T (p.Gly360Val) rs35993958
NM_000546.6(TP53):c.1100+8A>G rs878854062
NM_000546.6(TP53):c.18A>G (p.Ser6=) rs573130482
NM_000546.6(TP53):c.215_216delinsGT (p.Pro72Arg) rs878854066
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.450A>C (p.Thr150=) rs754020850
NM_000546.6(TP53):c.456G>A (p.Pro152=) rs876659481
NM_000546.6(TP53):c.559+8G>A rs775915220
NM_000546.6(TP53):c.672+9T>C rs1057521030
NM_000546.6(TP53):c.919+8A>C rs1555525043
NM_000546.6(TP53):c.924G>C (p.Leu308=) rs786202546
NM_000546.6(TP53):c.993+7A>G rs1023206153

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