List of variants in gene TP53 reported by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.*1175A>C	rs78378222	0.00849
NM_000546.6(TP53):c.782+17C>T	rs17880172	0.00184
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
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.935C>G (p.Thr312Ser)	rs145151284	0.00018
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_000546.6(TP53):c.903A>G (p.Pro301=)	rs72661120	0.00007
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.510G>A (p.Thr170=)	rs757544615	0.00002
NM_000546.6(TP53):c.145G>A (p.Asp49Asn)	rs587780728	0.00001
NM_000546.6(TP53):c.222C>T (p.Ala74=)	rs786201577	0.00001
NM_000546.6(TP53):c.524G>A (p.Arg175His)	rs28934578	0.00001
NM_000546.6(TP53):c.606T>C (p.Arg202=)	rs1392931620	0.00001
NM_000546.6(TP53):c.974G>T (p.Gly325Val)	rs121912659	0.00001
NM_000546.6(TP53):c.74+50_74+55dup	rs2073512697

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