ClinVar Miner

List of variants in gene TP53 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.173C>G (p.Pro58Arg) rs144386518 0.00030
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578 0.00028
NM_000546.6(TP53):c.704A>G (p.Asn235Ser) rs144340710 0.00025
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284 0.00018
NM_000546.6(TP53):c.217G>A (p.Val73Met) rs587782423 0.00011
NM_000546.6(TP53):c.97-9C>T rs202217267 0.00011
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys) rs17882252 0.00006
NM_000546.6(TP53):c.248C>T (p.Ala83Val) rs201717599 0.00006
NM_000546.6(TP53):c.*6T>A rs369567704 0.00005
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala) rs17881470 0.00004
NM_000546.6(TP53):c.1149C>T (p.Leu383=) rs373710656 0.00004
NM_000546.6(TP53):c.246G>A (p.Pro82=) rs372397095 0.00004
NM_000546.6(TP53):c.469G>A (p.Val157Ile) rs121912654 0.00004
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350 0.00004
NM_000546.6(TP53):c.180A>C (p.Pro60=) rs749289195 0.00003
NM_000546.6(TP53):c.188C>G (p.Ala63Gly) rs372201428 0.00003
NM_000546.6(TP53):c.30C>T (p.Val10=) rs568171603 0.00003
NM_000546.6(TP53):c.18A>C (p.Ser6=) rs573130482 0.00002
NM_000546.6(TP53):c.249G>A (p.Ala83=) rs55754907 0.00002
NM_000546.6(TP53):c.464C>G (p.Thr155Ser) rs786202752 0.00002
NM_000546.6(TP53):c.612G>A (p.Glu204=) rs749629973 0.00002
NM_000546.6(TP53):c.732C>T (p.Gly244=) rs759625762 0.00002
NM_000546.6(TP53):c.123T>C (p.Asp41=) rs369129220 0.00001
NM_000546.6(TP53):c.144C>T (p.Asp48=) rs587781460 0.00001
NM_000546.6(TP53):c.21T>A (p.Asp7Glu) rs587781277 0.00001
NM_000546.6(TP53):c.245C>T (p.Pro82Leu) rs534447939 0.00001
NM_000546.6(TP53):c.270C>T (p.Ser90=) rs863224370 0.00001
NM_000546.6(TP53):c.566C>T (p.Ala189Val) rs121912665 0.00001
NM_000546.6(TP53):c.885T>C (p.Pro295=) rs200073907 0.00001
NM_000546.6(TP53):c.168A>G (p.Glu56=) rs574255227
NM_000546.6(TP53):c.210T>C (p.Ala70=) rs786203513
NM_000546.6(TP53):c.30C>G (p.Val10=) rs568171603
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.456G>A (p.Pro152=) rs876659481
NM_000546.6(TP53):c.483C>A (p.Ala161=) rs1057523101
NM_000546.6(TP53):c.996C>T (p.Ile332=) rs1555524470

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