List of variants in gene TP53 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.993+12T>C	rs1800899	0.01614
NM_000546.6(TP53):c.376-117G>A	rs35850753	0.01308
NM_000546.6(TP53):c.376-86T>C	rs113530090	0.00891
NM_000546.6(TP53):c.672+31A>G	rs34949160	0.00543
NM_000546.6(TP53):c.673-100C>T	rs183276131	0.00414
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.672+18G>C	rs199578278	0.00014
NM_000546.6(TP53):c.28G>A (p.Val10Ile)	rs535274413	0.00004
NM_000546.6(TP53):c.375+17G>A	rs765179201
NM_000546.6(TP53):c.672+48G>T	rs17884607
NM_000546.6(TP53):c.894G>A (p.Glu298=)	rs756123992

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