ClinVar Miner

List of variants in gene TP53 studied for Acute myeloid leukemia

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NM_000546.6(TP53):c.-29+5139C>A rs181106784 0.00072
NM_000546.6(TP53):c.-29+5029A>G rs2073795533 0.00001
NM_000546.6(TP53):c.824G>A (p.Cys275Tyr) rs863224451 0.00001
NM_000546.6(TP53):c.-29+4907G>T rs1316311026
NM_000546.6(TP53):c.-29+4908G>C rs1418273116
NM_000546.6(TP53):c.-29+4914G>T rs1442908719
NM_000546.6(TP53):c.-29+4915del rs2530198874
NM_000546.6(TP53):c.-29+4952G>C rs2543699850
NM_000546.6(TP53):c.-29+5027A>T rs1381789291
NM_000546.6(TP53):c.323_329dup (p.Leu111fs) rs1131691004
NM_000546.6(TP53):c.331del (p.Leu111fs) rs2151039122
NM_000546.6(TP53):c.449C>T (p.Thr150Ile) rs2151032692
NM_000546.6(TP53):c.494A>T (p.Gln165Leu) rs2151031435
NM_000546.6(TP53):c.513G>T (p.Glu171Asp) rs1555526078
NM_000546.6(TP53):c.537T>A (p.His179Gln) rs876660821
NM_000546.6(TP53):c.549A>T (p.Ser183=) rs1597369559
NM_000546.6(TP53):c.576del (p.Gln192fs) rs2543588023
NM_000546.6(TP53):c.710T>A (p.Met237Lys) rs765848205
NM_000546.6(TP53):c.719G>A (p.Ser240Asn) rs2073256828
NM_000546.6(TP53):c.752T>A (p.Ile251Asn) rs730882027
NM_000546.6(TP53):c.761T>C (p.Ile254Thr) rs1330865474
NM_000546.6(TP53):c.800G>C (p.Arg267Pro) rs587780075
NM_000546.6(TP53):c.801G>C (p.Arg267=) rs1597362195
NM_000546.6(TP53):c.805A>T (p.Ser269Cys) rs1597362155
NM_000546.6(TP53):c.806G>T (p.Ser269Ile) rs2543545959
NM_000546.6(TP53):c.839G>C (p.Arg280Thr) rs121912660
NM_000546.6(TP53):c.952C>T (p.Pro318Ser) rs2151011743
NM_000546.6(TP53):c.954A>T (p.Pro318=) rs761322293
NM_000546.6(TP53):c.969G>C (p.Leu323=) rs672601297
NM_000546.6(TP53):c.970G>A (p.Asp324Asn) rs1064794810
NM_000546.6(TP53):c.977A>T (p.Glu326Val) rs2151011218
NM_000546.6(TP53):c.978A>G (p.Glu326=) rs1000256867
NM_000546.6(TP53):c.993+13G>A rs369599972
NM_000546.6(TP53):c.993+44C>A rs2151010166
NM_000546.6(TP53):c.993+86del rs2543520598

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