List of variants in gene TP53 reported as likely pathogenic by deCODE genetics, Amgen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.148dup (p.Ile50fs)	rs1567556956
NM_000546.6(TP53):c.430C>T (p.Gln144Ter)	rs757274881
NM_000546.6(TP53):c.437G>A (p.Trp146Ter)	rs1206165503
NM_000546.6(TP53):c.489_495del (p.Lys164fs)	rs2543598421
NM_000546.6(TP53):c.96+1G>C	rs1131691003

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