List of variants in gene TP53 reported as uncertain significance 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: 33

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.*1132C>T	rs1044102603	0.00035
NM_000546.6(TP53):c.*760T>C	rs935743951	0.00010
NM_000546.6(TP53):c.*144G>A	rs371002418	0.00007
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys)	rs17882252	0.00006
NM_000546.6(TP53):c.782+12C>T	rs17881780	0.00005
NM_000546.6(TP53):c.*327C>T	rs886053512	0.00002
NM_000546.6(TP53):c.*626C>T	rs886053506	0.00001
NM_000546.6(TP53):c.-22G>A	rs1348969852	0.00001
NM_000546.6(TP53):c.1093C>T (p.His365Tyr)	rs267605075	0.00001
NM_000546.6(TP53):c.145G>A (p.Asp49Asn)	rs587780728	0.00001
NM_000546.6(TP53):c.74+9A>C	rs1057517593	0.00001
NM_000546.6(TP53):c.96+15T>C	rs200053580	0.00001
NM_000546.6(TP53):c.*1160T>G	rs886053499
NM_000546.6(TP53):c.*168C>T	rs2072818956
NM_000546.6(TP53):c.*346G>T	rs886053511
NM_000546.6(TP53):c.*347T>C	rs886053510
NM_000546.6(TP53):c.*382C>T	rs886053509
NM_000546.6(TP53):c.*548G>T	rs886053508
NM_000546.6(TP53):c.*565G>T	rs886053507
NM_000546.6(TP53):c.*735C>A	rs886053505
NM_000546.6(TP53):c.*747C>T	rs886053504
NM_000546.6(TP53):c.*754C>T	rs199729221
NM_000546.6(TP53):c.*761T>C	rs925506797
NM_000546.6(TP53):c.*772del	rs200757381
NM_000546.6(TP53):c.*779del	rs886053503
NM_000546.6(TP53):c.*790G>A	rs886053502
NM_000546.6(TP53):c.*806C>A	rs886053501
NM_000546.6(TP53):c.*977G>C	rs886053500
NM_000546.6(TP53):c.*99G>A	rs886053513
NM_000546.6(TP53):c.145G>C (p.Asp49His)	rs587780728
NM_000546.6(TP53):c.31G>C (p.Glu11Gln)	rs201382018
NM_000546.6(TP53):c.63C>T (p.Asp21=)	rs1800369
NM_000546.6(TP53):c.993+8G>A	rs1060504163

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