List of variants in gene TP53 reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000546.5(TP53):c.319T>C (p.Tyr107His)	rs368771578	0.00028
NM_000546.6(TP53):c.1079G>C (p.Gly360Ala)	rs35993958	0.00019
NM_000546.6(TP53):c.869G>A (p.Arg290His)	rs55819519	0.00014
NM_000546.6(TP53):c.743G>A (p.Arg248Gln)	rs11540652	0.00002
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.733G>A (p.Gly245Ser)	rs28934575	0.00001
NM_000546.6(TP53):c.817C>T (p.Arg273Cys)	rs121913343	0.00001
NM_000546.6(TP53):c.844C>T (p.Arg282Trp)	rs28934574	0.00001
NM_000546.6(TP53):c.216dup (p.Val73fs)	rs730882018
NM_000546.6(TP53):c.377A>G (p.Tyr126Cys)	rs1555526335
NM_000546.6(TP53):c.481G>A (p.Ala161Thr)	rs193920817
NM_000546.6(TP53):c.532C>G (p.His178Asp)	rs1064795203
NM_000546.6(TP53):c.638G>A (p.Arg213Gln)	rs587778720
NM_000546.6(TP53):c.742C>T (p.Arg248Trp)	rs121912651
NM_000546.6(TP53):c.91G>T (p.Val31Phe)	rs201753350

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