List of variants reported as likely pathogenic for bone cancer by Ayesha Lab, University of the Punjab

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.824G>A (p.Cys275Tyr)	rs863224451	0.00001
NM_000546.6(TP53):c.800G>C (p.Arg267Pro)	rs587780075
NM_000546.6(TP53):c.801G>C (p.Arg267=)
NM_000546.6(TP53):c.806G>T (p.Ser269Ile)
NM_000546.6(TP53):c.839G>C (p.Arg280Thr)	rs121912660
NM_000546.6(TP53):c.977A>T (p.Glu326Val)

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