List of variants in gene TP53 reported as likely benign by Counsyl

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.994-17C>T	rs368691910	0.00087
NM_000546.6(TP53):c.704A>G (p.Asn235Ser)	rs144340710	0.00025
NM_000546.6(TP53):c.1079G>C (p.Gly360Ala)	rs35993958	0.00019
NM_000546.6(TP53):c.74+14T>C	rs184743157	0.00018
NM_000546.6(TP53):c.672+18G>C	rs199578278	0.00014
NM_000546.6(TP53):c.673-37C>T	rs374907737	0.00010
NM_000546.6(TP53):c.6G>A (p.Glu2=)	rs143458271	0.00009
NM_000546.6(TP53):c.97-28T>A	rs200989844	0.00006
NM_000546.6(TP53):c.993+234G>A	rs17883348	0.00006
NM_000546.6(TP53):c.782+12C>T	rs17881780	0.00005
NM_000546.6(TP53):c.1149C>T (p.Leu383=)	rs373710656	0.00004
NM_000546.6(TP53):c.255T>C (p.Pro85=)	rs775515332	0.00004
NM_000546.6(TP53):c.376-18dup	rs756417643	0.00004
NM_000546.6(TP53):c.672+15T>C	rs140756213	0.00004
NM_000546.6(TP53):c.993+227A>C	rs764562217	0.00004
NM_000546.6(TP53):c.180A>C (p.Pro60=)	rs749289195	0.00003
NM_000546.6(TP53):c.30C>T (p.Val10=)	rs568171603	0.00003
NM_000546.6(TP53):c.234A>G (p.Ala78=)	rs375099397	0.00002
NM_000546.6(TP53):c.249G>A (p.Ala83=)	rs55754907	0.00002
NM_000546.6(TP53):c.1023C>T (p.Phe341=)	rs864622369	0.00001
NM_000546.6(TP53):c.222C>T (p.Ala74=)	rs786201577	0.00001
NM_000546.6(TP53):c.408A>G (p.Gln136=)	rs758781593	0.00001
NM_000546.6(TP53):c.74+9A>C	rs1057517593	0.00001
NM_000546.6(TP53):c.885T>C (p.Pro295=)	rs200073907	0.00001
NM_000546.6(TP53):c.97-15T>C	rs1555526843	0.00001
NM_000546.6(TP53):c.993+290T>C	rs1642789	0.00001
NM_000546.6(TP53):c.375+17G>A	rs765179201
NM_000546.6(TP53):c.666G>T (p.Pro222=)	rs72661118
NM_000546.6(TP53):c.768A>G (p.Thr256=)	rs786203563
NM_000546.6(TP53):c.783-13C>G	rs1555525373
NM_000546.6(TP53):c.787A>G (p.Asn263Asp)	rs72661119
NM_000546.6(TP53):c.993+223T>G	rs3021068
NM_000546.6(TP53):c.993+244G>A	rs576532147
NM_000546.6(TP53):c.993+312_993+314del	rs1555524872
NM_000546.6(TP53):c.993+326_993+341del	rs730882013

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