ClinVar Miner

List of variants reported as likely benign for malignant mixed neoplasm by All of Us Research Program, National Institutes of Health

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.1140C>A (p.Ala380=) rs147126640 0.00008
NM_024426.6(WT1):c.1020C>T (p.His340=) rs375114529 0.00007
NM_024426.6(WT1):c.1146T>A (p.Thr382=) rs371168589 0.00006
NM_024426.6(WT1):c.117G>A (p.Arg39=) rs537150542 0.00006
NM_024426.6(WT1):c.1269G>A (p.Glu423=) rs767850636 0.00006
NM_024426.6(WT1):c.510C>T (p.Ser170=) rs772890986 0.00005
NM_024426.6(WT1):c.813G>C (p.Pro271=) rs1341857958 0.00004
NM_024426.6(WT1):c.273G>A (p.Leu91=) rs1396104394 0.00003
NM_024426.6(WT1):c.327G>C (p.Pro109=) rs777059515 0.00003
NM_024426.6(WT1):c.432C>T (p.Phe144=) rs754173303 0.00003
NM_024426.6(WT1):c.1563G>A (p.Ala521=) rs202118284 0.00002
NM_024426.6(WT1):c.159C>T (p.Ala53=) rs1021307133 0.00002
NM_024426.6(WT1):c.198G>T (p.Ala66=) rs955105743 0.00002
NM_024426.6(WT1):c.627C>T (p.Ser209=) rs761530541 0.00002
NM_024426.6(WT1):c.711C>T (p.Pro237=) rs183263057 0.00002
NM_024426.6(WT1):c.78G>A (p.Gly26=) rs1240715155 0.00002
NM_024426.6(WT1):c.996A>G (p.Lys332=) rs758410591 0.00002
NM_024426.6(WT1):c.1008G>A (p.Gly336=) rs1369099437 0.00001
NM_024426.6(WT1):c.1029G>A (p.Gly343=) rs752102247 0.00001
NM_024426.6(WT1):c.1035G>A (p.Glu345=) rs757962229 0.00001
NM_024426.6(WT1):c.1053G>A (p.Thr351=) rs1260693060 0.00001
NM_024426.6(WT1):c.1434T>C (p.His478=) rs761414130 0.00001
NM_024426.6(WT1):c.1448-7T>C rs1392191365 0.00001
NM_024426.6(WT1):c.186G>A (p.Arg62=) rs1294714508 0.00001
NM_024426.6(WT1):c.366G>A (p.Gly122=) rs1362739411 0.00001
NM_024426.6(WT1):c.429C>G (p.Ser143=) rs531076591 0.00001
NM_024426.6(WT1):c.480G>A (p.Gln160=) rs758900425 0.00001
NM_024426.6(WT1):c.549G>A (p.Gly183=) rs1199167878 0.00001
NM_024426.6(WT1):c.54G>A (p.Ala18=) rs1409626312 0.00001
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095 0.00001
NM_024426.6(WT1):c.619C>T (p.Leu207=) rs1060504180 0.00001
NM_024426.6(WT1):c.81T>C (p.Pro27=) rs755007049 0.00001
NM_024426.6(WT1):c.846C>T (p.Cys282=) rs1281989931 0.00001
NM_024426.6(WT1):c.1026A>C (p.Thr342=)
NM_024426.6(WT1):c.1041T>C (p.Asp347=) rs1159089816
NM_024426.6(WT1):c.1056C>T (p.Pro352=) rs2132958298
NM_024426.6(WT1):c.1114-14CT[2] rs994248697
NM_024426.6(WT1):c.1143G>A (p.Pro381=) rs1554939849
NM_024426.6(WT1):c.1200C>T (p.Tyr400=) rs886048227
NM_024426.6(WT1):c.1265-4C>T rs918343735
NM_024426.6(WT1):c.1329C>A (p.Leu443=)
NM_024426.6(WT1):c.1419C>G (p.Thr473=)
NM_024426.6(WT1):c.1476A>G (p.Pro492=) rs2132899419
NM_024426.6(WT1):c.204G>A (p.Gly68=) rs1554946680
NM_024426.6(WT1):c.228C>G (p.Ser76=)
NM_024426.6(WT1):c.237G>A (p.Arg79=)
NM_024426.6(WT1):c.24C>T (p.Asp8=)
NM_024426.6(WT1):c.259G>A (p.Ala87Thr) rs752686863
NM_024426.6(WT1):c.261C>G (p.Ala87=)
NM_024426.6(WT1):c.267C>T (p.Pro89=) rs1172336462
NM_024426.6(WT1):c.288C>G (p.Gly96=)
NM_024426.6(WT1):c.312G>A (p.Ala104=) rs1590410376
NM_024426.6(WT1):c.318G>A (p.Gln106=)
NM_024426.6(WT1):c.327G>A (p.Pro109=)
NM_024426.6(WT1):c.363C>T (p.Tyr121=) rs977632626
NM_024426.6(WT1):c.408C>T (p.Pro136=)
NM_024426.6(WT1):c.429C>T (p.Ser143=) rs531076591
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.471C>T (p.His157=) rs753238865
NM_024426.6(WT1):c.522T>G (p.Thr174=)
NM_024426.6(WT1):c.564T>A (p.Pro188=) rs1060504178
NM_024426.6(WT1):c.579G>A (p.Ala193=) rs2133101885
NM_024426.6(WT1):c.651T>C (p.Ile217=)
NM_024426.6(WT1):c.662-13G>A
NM_024426.6(WT1):c.662-14C>T
NM_024426.6(WT1):c.66G>C (p.Thr22=)
NM_024426.6(WT1):c.675C>A (p.Val225=)
NM_024426.6(WT1):c.690G>T (p.Thr230=)
NM_024426.6(WT1):c.699C>T (p.Tyr233=) rs1349302999
NM_024426.6(WT1):c.708G>A (p.Thr236=) rs768828897
NM_024426.6(WT1):c.723G>A (p.Ala241=)
NM_024426.6(WT1):c.777C>G (p.Gly259=)
NM_024426.6(WT1):c.785-14G>C rs375514482
NM_024426.6(WT1):c.785-15C>T
NM_024426.6(WT1):c.789G>A (p.Glu263=) rs878855087
NM_024426.6(WT1):c.792G>A (p.Gln264=)
NM_024426.6(WT1):c.801G>C (p.Ser267=)
NM_024426.6(WT1):c.837C>T (p.Thr279=) rs747613465
NM_024426.6(WT1):c.849C>G (p.Thr283=)
NM_024426.6(WT1):c.876G>A (p.Thr292=) rs1343218741
NM_024426.6(WT1):c.876G>T (p.Thr292=) rs1343218741
NM_024426.6(WT1):c.966-11T>C
NM_024426.6(WT1):c.966-9C>G
NM_024426.6(WT1):c.99A>G (p.Pro33=) rs2133107306

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