ClinVar Miner

List of variants reported as likely benign for Li-Fraumeni syndrome 1 by Counsyl

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Total variants: 35
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HGVS dbSNP
NM_000546.5(TP53):c.1023C>T (p.Phe341=) rs864622369
NM_000546.5(TP53):c.1079G>C (p.Gly360Ala) rs35993958
NM_000546.5(TP53):c.1149C>T (p.Leu383=) rs373710656
NM_000546.5(TP53):c.180A>C (p.Pro60=) rs749289195
NM_000546.5(TP53):c.222C>T (p.Ala74=) rs786201577
NM_000546.5(TP53):c.234A>G (p.Ala78=) rs375099397
NM_000546.5(TP53):c.249G>A (p.Ala83=) rs55754907
NM_000546.5(TP53):c.255T>C (p.Pro85=) rs775515332
NM_000546.5(TP53):c.30C>T (p.Val10=) rs568171603
NM_000546.5(TP53):c.375+17G>A rs765179201
NM_000546.5(TP53):c.376-18dup rs756417643
NM_000546.5(TP53):c.408A>G (p.Gln136=) rs758781593
NM_000546.5(TP53):c.666G>T (p.Pro222=) rs72661118
NM_000546.5(TP53):c.672+15T>C rs140756213
NM_000546.5(TP53):c.672+18G>C rs199578278
NM_000546.5(TP53):c.673-37C>T rs374907737
NM_000546.5(TP53):c.6G>A (p.Glu2=) rs143458271
NM_000546.5(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_000546.5(TP53):c.74+14T>C rs184743157
NM_000546.5(TP53):c.74+9A>C rs1057517593
NM_000546.5(TP53):c.768A>G (p.Thr256=) rs786203563
NM_000546.5(TP53):c.782+12C>T rs17881780
NM_000546.5(TP53):c.783-13C>G rs1555525373
NM_000546.5(TP53):c.787A>G (p.Asn263Asp) rs72661119
NM_000546.5(TP53):c.885T>C (p.Pro295=) rs200073907
NM_000546.5(TP53):c.97-15T>C rs1555526843
NM_000546.5(TP53):c.97-28T>A rs200989844
NM_000546.5(TP53):c.993+234G>A rs17883348
NM_000546.5(TP53):c.993+244G>A rs576532147
NM_000546.5(TP53):c.993+326_993+341del rs730882013
NM_000546.5(TP53):c.994-17C>T rs368691910
NM_001126113.2(TP53):c.1015T>C (p.Cys339Arg) rs1642789
NM_001126113.2(TP53):c.1034_1036CGT[1] (p.Ser346del) rs1555524872
NM_001126114.2(TP53):c.1021T>G (p.Cys341Gly) rs3021068
NM_001126114.2(TP53):c.1025A>C (p.Ter342Ser) rs764562217

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