ClinVar Miner

List of variants in gene TP53 reported as likely benign by Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine

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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.883C>T (p.Pro295Ser) rs1131691006 0.00004
NM_000546.6(TP53):c.382C>A (p.Pro128Thr) rs1555526327 0.00003
NM_000546.6(TP53):c.1004G>A (p.Arg335His) rs771939956 0.00001
NM_000546.6(TP53):c.1027G>C (p.Glu343Gln) rs375573770 0.00001
NM_000546.6(TP53):c.1061A>G (p.Gln354Arg) rs752142489 0.00001
NM_000546.6(TP53):c.1082G>A (p.Gly361Glu) rs587781663 0.00001
NM_000546.6(TP53):c.1085G>T (p.Ser362Ile) rs768803947 0.00001
NM_000546.6(TP53):c.1133C>G (p.Ser378Cys) rs1555524130 0.00001
NM_000546.6(TP53):c.1165G>A (p.Gly389Arg) rs587783064 0.00001
NM_000546.6(TP53):c.171C>A (p.Asp57Glu) rs587782776 0.00001
NM_000546.6(TP53):c.26G>A (p.Ser9Asn) rs1555527015 0.00001
NM_000546.6(TP53):c.37C>T (p.Pro13Ser) rs1060501208 0.00001
NM_000546.6(TP53):c.38C>T (p.Pro13Leu) rs878854070 0.00001
NM_000546.6(TP53):c.457C>T (p.Pro153Ser) rs1064795860 0.00001
NM_000546.6(TP53):c.4G>A (p.Glu2Lys) rs769884991 0.00001
NM_000546.6(TP53):c.559G>A (p.Gly187Ser) rs776167460 0.00001
NM_000546.6(TP53):c.649G>A (p.Val217Met) rs35163653 0.00001
NM_000546.6(TP53):c.686G>A (p.Cys229Tyr) rs1064793603 0.00001
NM_000546.6(TP53):c.694A>C (p.Ile232Leu) rs1555525562 0.00001
NM_000546.6(TP53):c.861G>C (p.Glu287Asp) rs748891343 0.00001
NM_000546.6(TP53):c.946C>A (p.Pro316Thr) rs772773208 0.00001
NM_000546.6(TP53):c.950A>G (p.Gln317Arg) rs1159579789 0.00001
NM_000546.6(TP53):c.953C>T (p.Pro318Leu) rs1555524975 0.00001
NM_000546.6(TP53):c.1036G>A (p.Glu346Lys) rs1567542019
NM_000546.6(TP53):c.1079G>A (p.Gly360Glu) rs35993958
NM_000546.6(TP53):c.107C>T (p.Pro36Leu) rs587781866
NM_000546.6(TP53):c.1084A>T (p.Ser362Cys) rs1287887419
NM_000546.6(TP53):c.1085G>A (p.Ser362Asn) rs768803947
NM_000546.6(TP53):c.1087A>G (p.Arg363Gly) rs745751553
NM_000546.6(TP53):c.1090G>T (p.Ala364Ser) rs2072906212
NM_000546.6(TP53):c.1118A>G (p.Lys373Arg) rs1567540504
NM_000546.6(TP53):c.1119G>T (p.Lys373Asn) rs1342613419
NM_000546.6(TP53):c.1120G>T (p.Gly374Cys) rs587781858
NM_000546.6(TP53):c.1129A>C (p.Thr377Pro) rs774269719
NM_000546.6(TP53):c.1135C>T (p.Arg379Cys) rs749061599
NM_000546.6(TP53):c.124G>A (p.Asp42Asn) rs756847009
NM_000546.6(TP53):c.129G>C (p.Leu43Phe) rs754332870
NM_000546.6(TP53):c.139C>A (p.Pro47Thr) rs1800371
NM_000546.6(TP53):c.147T>G (p.Asp49Glu) rs786201148
NM_000546.6(TP53):c.182A>G (p.Asp61Gly) rs1460793472
NM_000546.6(TP53):c.211C>G (p.Pro71Ala) rs1567556576
NM_000546.6(TP53):c.229C>A (p.Pro77Thr) rs753085009
NM_000546.6(TP53):c.233C>G (p.Ala78Gly) rs876658527
NM_000546.6(TP53):c.242C>T (p.Thr81Ile) rs1567556386
NM_000546.6(TP53):c.244C>G (p.Pro82Ala) rs1555526664
NM_000546.6(TP53):c.260C>T (p.Pro87Leu) rs2073467677
NM_000546.6(TP53):c.263C>T (p.Ala88Val) rs1555526631
NM_000546.6(TP53):c.266C>T (p.Pro89Leu) rs730881994
NM_000546.6(TP53):c.275C>T (p.Pro92Leu) rs1210700121
NM_000546.6(TP53):c.289G>C (p.Val97Leu) rs730882023
NM_000546.6(TP53):c.29T>G (p.Val10Gly) rs1418778734
NM_000546.6(TP53):c.305C>T (p.Thr102Ile) rs786202717
NM_000546.6(TP53):c.317G>T (p.Ser106Ile) rs1567555883
NM_000546.6(TP53):c.322G>T (p.Gly108Cys) rs587782461
NM_000546.6(TP53):c.334G>A (p.Gly112Ser) rs1423803759
NM_000546.6(TP53):c.35C>G (p.Pro12Arg) rs1482497533
NM_000546.6(TP53):c.442G>T (p.Asp148Tyr) rs1131691007
NM_000546.6(TP53):c.625A>G (p.Arg209Gly) rs1429743956
NM_000546.6(TP53):c.672G>T (p.Glu224Asp) rs267605076
NM_000546.6(TP53):c.686G>C (p.Cys229Ser) rs1064793603
NM_000546.6(TP53):c.727A>G (p.Met243Val) rs786203117
NM_000546.6(TP53):c.850A>G (p.Thr284Ala) rs1204379654
NM_000546.6(TP53):c.892G>C (p.Glu298Gln) rs201744589
NM_000546.6(TP53):c.910A>G (p.Thr304Ala) rs587782654
NM_000546.6(TP53):c.925C>T (p.Pro309Ser) rs1555525012
NM_000546.6(TP53):c.930C>A (p.Asn310Lys) rs876660829
NM_000546.6(TP53):c.941C>T (p.Ser314Phe) rs751440465
NM_000546.6(TP53):c.946C>T (p.Pro316Ser) rs772773208
NM_000546.6(TP53):c.964C>T (p.Pro322Ser) rs863224687

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