ClinVar Miner

List of variants in gene TP53 reported by MutSpliceDB: a database of splice sites variants effects on splicing, NIH

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.375G>A (p.Thr125=) rs55863639 0.00001
NM_000546.6(TP53):c.376-1G>A rs868137297 0.00001
NM_000546.6(TP53):c.560-1G>A rs1202793339 0.00001
NM_000546.6(TP53):c.783-1G>A rs1555525367 0.00001
NM_000546.6(TP53):c.1101-2A>C rs587781664
NM_000546.6(TP53):c.1101-2A>G rs587781664
NM_000546.6(TP53):c.1101-2A>T rs587781664
NM_000546.6(TP53):c.375+1G>A rs1567555445
NM_000546.6(TP53):c.375+1G>T rs1567555445
NM_000546.6(TP53):c.375+1del
NM_000546.6(TP53):c.375+2T>C rs1555526469
NM_000546.6(TP53):c.375+2T>G rs1555526469
NM_000546.6(TP53):c.375+5G>A rs1555526466
NM_000546.6(TP53):c.375G>C (p.Thr125=) rs55863639
NM_000546.6(TP53):c.375G>T (p.Thr125=) rs55863639
NM_000546.6(TP53):c.376-1G>C
NM_000546.6(TP53):c.376-1G>T rs868137297
NM_000546.6(TP53):c.376-2A>C rs786202799
NM_000546.6(TP53):c.376-2A>G rs786202799
NM_000546.6(TP53):c.376-2A>T rs786202799
NM_000546.6(TP53):c.559+1G>A rs1131691042
NM_000546.6(TP53):c.559+1G>T rs1131691042
NM_000546.6(TP53):c.559+2T>A rs1597369404
NM_000546.6(TP53):c.559G>C (p.Gly187Arg) rs776167460
NM_000546.6(TP53):c.560-1G>C rs1202793339
NM_000546.6(TP53):c.560-2A>C rs1427441061
NM_000546.6(TP53):c.672+1G>A rs863224499
NM_000546.6(TP53):c.672+1G>T rs863224499
NM_000546.6(TP53):c.672+2T>A rs1555525703
NM_000546.6(TP53):c.672+2T>C rs1555525703
NM_000546.6(TP53):c.672+2T>G rs1555525703
NM_000546.6(TP53):c.672G>A (p.Glu224=) rs267605076
NM_000546.6(TP53):c.672G>T (p.Glu224Asp) rs267605076
NM_000546.6(TP53):c.673-1G>A rs878854073
NM_000546.6(TP53):c.673-1G>C rs878854073
NM_000546.6(TP53):c.673-1G>T rs878854073
NM_000546.6(TP53):c.673-2A>C rs1555525585
NM_000546.6(TP53):c.673-2A>G rs1555525585
NM_000546.6(TP53):c.673-2A>T rs1555525585
NM_000546.6(TP53):c.75-1G>T rs2151045740
NM_000546.6(TP53):c.75-2A>G rs1131691020
NM_000546.6(TP53):c.782+1G>A rs1555525429
NM_000546.6(TP53):c.782+1G>T rs1555525429
NM_000546.6(TP53):c.782+2T>G rs876659076
NM_000546.6(TP53):c.782G>C (p.Ser261Thr) rs786203396
NM_000546.6(TP53):c.783-1G>T rs1555525367
NM_000546.6(TP53):c.783-2A>C rs1060501207
NM_000546.6(TP53):c.783-2A>T rs1060501207
NM_000546.6(TP53):c.919+1G>A rs1131691039
NM_000546.6(TP53):c.919+1G>C rs1131691039
NM_000546.6(TP53):c.919+1G>T
NM_000546.6(TP53):c.919+2T>G rs1131691016
NM_000546.6(TP53):c.920-1G>A rs587781702
NM_000546.6(TP53):c.920-1G>T rs587781702
NM_000546.6(TP53):c.920-2A>G rs397516439
NM_000546.6(TP53):c.96+1G>A rs1131691003
NM_000546.6(TP53):c.96+1G>T rs1131691003
NM_000546.6(TP53):c.97-1G>A rs1597375294
NM_000546.6(TP53):c.993+1G>A rs11575997
NM_000546.6(TP53):c.993+1G>C rs11575997
NM_000546.6(TP53):c.993+1G>T rs11575997
NM_000546.6(TP53):c.993+2T>C rs1597359053
NM_000546.6(TP53):c.993+2T>G rs1597359053
NM_000546.6(TP53):c.993G>A (p.Gln331=) rs11575996
NM_000546.6(TP53):c.994-1G>A rs587782272
NM_000546.6(TP53):c.994-1G>C rs587782272
NM_000546.6(TP53):c.994-1G>T rs587782272
NM_000546.6(TP53):c.994-2A>C rs867389695
NM_000546.6(TP53):c.994-2A>G rs867389695
NM_000546.6(TP53):c.994-2A>T rs867389695

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