List of variants in gene TP53 reported by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.743G>A (p.Arg248Gln)	rs11540652	0.00002
NM_000546.6(TP53):c.375G>A (p.Thr125=)	rs55863639	0.00001
NM_000546.6(TP53):c.473G>A (p.Arg158His)	rs587782144	0.00001
NM_000546.6(TP53):c.817C>T (p.Arg273Cys)	rs121913343	0.00001
NM_000546.6(TP53):c.272G>A (p.Trp91Ter)	rs2073465664
NM_000546.6(TP53):c.365_366del (p.Val122fs)	rs587780067
NM_000546.6(TP53):c.451C>A (p.Pro151Thr)	rs28934874
NM_000546.6(TP53):c.451C>T (p.Pro151Ser)	rs28934874
NM_000546.6(TP53):c.455dup (p.Pro153fs)	rs730882019
NM_000546.6(TP53):c.560-1G>C	rs1202793339
NM_000546.6(TP53):c.638G>A (p.Arg213Gln)	rs587778720
NM_000546.6(TP53):c.730G>A (p.Gly244Ser)	rs1057519989
NM_000546.6(TP53):c.794T>C (p.Leu265Pro)	rs879253942
NM_000546.6(TP53):c.818G>A (p.Arg273His)	rs28934576
NM_000546.6(TP53):c.845G>A (p.Arg282Gln)	rs730882008
NM_000546.6(TP53):c.892G>T (p.Glu298Ter)	rs201744589

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