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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.173C>G (p.Pro58Arg)	rs144386518	0.00030
NM_000546.6(TP53):c.1079G>C (p.Gly360Ala)	rs35993958	0.00019
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys)	rs17882252	0.00006
NM_000546.6(TP53):c.618G>A (p.Leu206=)	rs142813240	0.00006
NM_000546.6(TP53):c.102C>G (p.Pro34=)	rs11575998	0.00004
NM_000546.6(TP53):c.246G>A (p.Pro82=)	rs372397095	0.00004
NM_000546.6(TP53):c.255T>C (p.Pro85=)	rs775515332	0.00004
NM_000546.6(TP53):c.469G>A (p.Val157Ile)	rs121912654	0.00004
NM_000546.6(TP53):c.180A>C (p.Pro60=)	rs749289195	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.468C>T (p.Arg156=)	rs761222871	0.00002
NM_000546.6(TP53):c.510G>A (p.Thr170=)	rs757544615	0.00002
NM_000546.6(TP53):c.582T>C (p.Leu194=)	rs370216745	0.00002
NM_000546.6(TP53):c.1025G>A (p.Arg342Gln)	rs375338359	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.270C>T (p.Ser90=)	rs863224370	0.00001
NM_000546.6(TP53):c.354A>T (p.Thr118=)	rs751978853	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.782+10C>T	rs200277687	0.00001
NM_000546.6(TP53):c.867C>T (p.Leu289=)	rs778138282	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.1079G>T (p.Gly360Val)	rs35993958
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.66A>G (p.Leu22=)	rs748527030
NM_000546.6(TP53):c.924G>C (p.Leu308=)	rs786202546

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