List of variants in gene TP53 reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.569_570del	rs1555523911	0.01175
NC_000017.11:g.7668388C>G	rs17883782	0.00356
NM_000546.6(TP53):c.*409C>A	rs191918079	0.00238
NM_000546.6(TP53):c.*357T>C	rs534624315	0.00192
NM_000546.6(TP53):c.*936A>G	rs55817367	0.00054
NM_000546.6(TP53):c.1014C>T (p.Phe338=)	rs150293825	0.00018
NM_000546.6(TP53):c.935C>G (p.Thr312Ser)	rs145151284	0.00018
NM_000546.6(TP53):c.91G>A (p.Val31Ile)	rs201753350	0.00009
NM_000546.6(TP53):c.18A>G (p.Ser6=)	rs573130482

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