List of variants in gene TP53 reported as uncertain significance by Sema4, Sema4

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_000546.6(TP53):c.998G>A (p.Arg333His)	rs573154688	0.00004
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.464C>G (p.Thr155Ser)	rs786202752	0.00002
NM_000546.6(TP53):c.466C>T (p.Arg156Cys)	rs563378859	0.00002
NM_000546.6(TP53):c.784G>A (p.Gly262Ser)	rs200579969	0.00002
NM_000546.6(TP53):c.572C>G (p.Pro191Arg)	rs587778718	0.00001
NM_000546.6(TP53):c.604C>T (p.Arg202Cys)	rs587780072	0.00001
NM_000546.6(TP53):c.783-10T>C	rs377590379	0.00001
NM_000546.6(TP53):c.800G>A (p.Arg267Gln)	rs587780075	0.00001
NM_000546.6(TP53):c.861G>C (p.Glu287Asp)	rs748891343	0.00001
NM_000546.6(TP53):c.920-9C>T	rs1265260122	0.00001
NM_000546.6(TP53):c.943T>A (p.Ser315Thr)	rs762620193	0.00001
NM_000546.6(TP53):c.949C>A (p.Gln317Lys)	rs764735889	0.00001
NM_000546.6(TP53):c.1003C>T (p.Arg335Cys)	rs375444154
NM_000546.6(TP53):c.129G>C (p.Leu43Phe)	rs754332870
NM_000546.6(TP53):c.215C>A (p.Pro72His)	rs1042522
NM_000546.6(TP53):c.234_263del (p.Ala79_Ala88del)	rs754312472
NM_000546.6(TP53):c.35C>G (p.Pro12Arg)	rs1482497533
NM_000546.6(TP53):c.375+4A>G	rs1060501192
NM_000546.6(TP53):c.376-4A>T	rs1221388024
NM_000546.6(TP53):c.415A>C (p.Lys139Gln)	rs1212996409
NM_000546.6(TP53):c.641A>C (p.His214Pro)	rs1057519992
NM_000546.6(TP53):c.652G>A (p.Val218Met)	rs878854072
NM_000546.6(TP53):c.783-4G>A	rs1060504160
NM_000546.6(TP53):c.870C>T (p.Arg290=)	rs1555525135
NM_000546.6(TP53):c.87C>G (p.Asn29Lys)	rs1011445550
NM_000546.6(TP53):c.920-14_920-3del	rs768598540
NM_000546.6(TP53):c.97-3C>T	rs786203749

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