List of variants in gene TP53 reported as uncertain significance by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.466C>T (p.Arg156Cys)	rs563378859	0.00002
NM_000546.6(TP53):c.523C>T (p.Arg175Cys)	rs138729528	0.00002
NM_000546.6(TP53):c.665C>T (p.Pro222Leu)	rs146340390	0.00002
NM_000546.6(TP53):c.328C>T (p.Arg110Cys)	rs587781371	0.00001
NM_000546.6(TP53):c.559G>A (p.Gly187Ser)	rs776167460	0.00001
NM_000546.6(TP53):c.427G>T (p.Val143Leu)	rs587782620
NM_000546.6(TP53):c.460G>C (p.Gly154Arg)	rs137852789
NM_000546.6(TP53):c.672+9T>C	rs1057521030
NM_000546.6(TP53):c.783-16T>G	rs2151017461
NM_000546.6(TP53):c.78_95dup (p.Leu32_Ser33insProGluAsnAsnValLeu)	rs2543641535
NM_000546.6(TP53):c.935C>T (p.Thr312Ile)	rs145151284

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