List of variants in gene TP53 reported as benign by Illumina Laboratory Services, Illumina

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: 14

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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.*773C>T	rs200378797	0.06166
NM_000546.6(TP53):c.*826G>A	rs17884306	0.05075
NM_000546.6(TP53):c.*485G>A	rs4968187	0.01815
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.639A>G (p.Arg213=)	rs1800372	0.01275
NM_000546.6(TP53):c.108G>A (p.Pro36=)	rs1800370	0.00974
NM_000546.6(TP53):c.*1175A>C	rs78378222	0.00849
NM_000546.6(TP53):c.97-6C>T	rs35117667	0.00847
NM_000546.6(TP53):c.*205G>A	rs16956880	0.00497
NM_000546.6(TP53):c.*328G>A	rs17881366	0.00463
NM_000546.6(TP53):c.*613C>A	rs17879353	0.00271
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
NM_000546.6(TP53):c.*1070C>T	rs114831472

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