ClinVar Miner

List of variants in gene MPL reported as likely benign for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP
NM_005373.2(MPL):c.*1054G>A rs139528456
NM_005373.2(MPL):c.*1116G>A rs144177827
NM_005373.2(MPL):c.*1126A>G rs543250497
NM_005373.2(MPL):c.*1180G>A rs117166528
NM_005373.2(MPL):c.*1486T>C rs149940158
NM_005373.2(MPL):c.*1506G>A rs115780311
NM_005373.2(MPL):c.*1603A>C rs142139493
NM_005373.2(MPL):c.*1674A>T rs536844021
NM_005373.2(MPL):c.*364C>T rs138892634
NM_005373.2(MPL):c.*400C>T rs558390922
NM_005373.2(MPL):c.*573G>A rs192016153
NM_005373.2(MPL):c.*662C>T rs1763698
NM_005373.2(MPL):c.*709C>T rs185654501
NM_005373.2(MPL):c.*748C>T rs190071085
NM_005373.2(MPL):c.*94C>A rs77858532
NM_005373.2(MPL):c.1003G>A (p.Glu335Lys) rs139770726
NM_005373.2(MPL):c.1102G>T (p.Val368Leu) rs149810307
NM_005373.2(MPL):c.1120A>G (p.Thr374Ala) rs190983971
NM_005373.2(MPL):c.117G>T (p.Lys39Asn) rs17292650
NM_005373.2(MPL):c.1467C>T (p.Thr489=) rs759161511
NM_005373.2(MPL):c.1565+5C>T rs41269541
NM_005373.2(MPL):c.1570C>T (p.Leu524=) rs146372205
NM_005373.2(MPL):c.1609C>T (p.Arg537Trp) rs148784027
NM_005373.2(MPL):c.1653+3G>A rs149625825
NM_005373.2(MPL):c.1654-10T>A rs200460456
NM_005373.2(MPL):c.1666G>T (p.Val556Phe) rs150004498
NM_005373.2(MPL):c.1794C>T (p.Cys598=) rs143457144
NM_005373.2(MPL):c.1803C>T (p.Thr601=) rs140794721
NM_005373.2(MPL):c.210G>A (p.Pro70=) rs6086
NM_005373.2(MPL):c.543T>C (p.Gly181=) rs17572791
NM_005373.2(MPL):c.549G>A (p.Thr183=) rs147130173
NM_005373.2(MPL):c.677C>A (p.Ser226Tyr) rs141063159
NM_005373.2(MPL):c.690+11C>T rs144769485
NM_005373.2(MPL):c.754T>C (p.Tyr252His) rs141311765
NM_005373.2(MPL):c.771C>A (p.Arg257=) rs1553127722
NM_005373.2(MPL):c.854-3T>C rs201514537
NM_005373.2(MPL):c.962G>A (p.Arg321Gln) rs149265851
NM_005373.3(MPL):c.1002C>T (p.Cys334=) rs141526418
NM_005373.3(MPL):c.1014G>A (p.Glu338=)
NM_005373.3(MPL):c.1023T>C (p.Asn341=)
NM_005373.3(MPL):c.1053C>T (p.Arg351=) rs753608517
NM_005373.3(MPL):c.1116G>A (p.Pro372=)
NM_005373.3(MPL):c.1119T>C (p.Gly373=) rs748581599
NM_005373.3(MPL):c.1134C>T (p.Tyr378=) rs749571171
NM_005373.3(MPL):c.1140C>G (p.Gly380=)
NM_005373.3(MPL):c.1165+10T>C
NM_005373.3(MPL):c.1165+8C>A
NM_005373.3(MPL):c.1166-4G>A rs753315546
NM_005373.3(MPL):c.1167G>A (p.Val389=)
NM_005373.3(MPL):c.1197G>A (p.Arg399=)
NM_005373.3(MPL):c.120T>C (p.Cys40=)
NM_005373.3(MPL):c.1242G>A (p.Ser414=)
NM_005373.3(MPL):c.1242G>C (p.Ser414=)
NM_005373.3(MPL):c.1308+8C>A
NM_005373.3(MPL):c.1308+8C>G
NM_005373.3(MPL):c.1309-6G>A
NM_005373.3(MPL):c.1320G>C (p.Pro440=)
NM_005373.3(MPL):c.1338A>G (p.Gly446=)
NM_005373.3(MPL):c.1356C>T (p.Arg452=)
NM_005373.3(MPL):c.1359G>A (p.Pro453=)
NM_005373.3(MPL):c.1401C>T (p.Gly467=)
NM_005373.3(MPL):c.1446G>A (p.Arg482=)
NM_005373.3(MPL):c.1455C>A (p.Thr485=) rs1420201893
NM_005373.3(MPL):c.1468+10G>A
NM_005373.3(MPL):c.1469-10T>C
NM_005373.3(MPL):c.1488C>T (p.Thr496=)
NM_005373.3(MPL):c.1536G>A (p.Leu512=)
NM_005373.3(MPL):c.1566-7C>T
NM_005373.3(MPL):c.1566-8T>C
NM_005373.3(MPL):c.1572G>C (p.Leu524=)
NM_005373.3(MPL):c.1573A>C (p.Arg525=)
NM_005373.3(MPL):c.1584G>A (p.Leu528=)
NM_005373.3(MPL):c.1629T>C (p.Leu543=)
NM_005373.3(MPL):c.1632G>A (p.Arg544=)
NM_005373.3(MPL):c.1635C>T (p.Asp545=)
NM_005373.3(MPL):c.1650C>T (p.Ser550=) rs377715574
NM_005373.3(MPL):c.1653+7G>A
NM_005373.3(MPL):c.1654-5C>A
NM_005373.3(MPL):c.1654-5C>T
NM_005373.3(MPL):c.1704T>C (p.Leu568=) rs1428589548
NM_005373.3(MPL):c.1719G>A (p.Lys573=)
NM_005373.3(MPL):c.174G>A (p.Ala58=) rs141077413
NM_005373.3(MPL):c.1773C>T (p.Tyr591=)
NM_005373.3(MPL):c.1809C>G (p.Pro603=)
NM_005373.3(MPL):c.1818G>A (p.Val606=)
NM_005373.3(MPL):c.198G>A (p.Leu66=)
NM_005373.3(MPL):c.231C>T (p.Cys77=) rs747378368
NM_005373.3(MPL):c.237G>C (p.Leu79=) rs769101640
NM_005373.3(MPL):c.255C>T (p.Pro85=)
NM_005373.3(MPL):c.273C>T (p.Tyr91=) rs759361904
NM_005373.3(MPL):c.279C>T (p.Cys93=)
NM_005373.3(MPL):c.27C>T (p.Val9=)
NM_005373.3(MPL):c.306T>A (p.Arg102=)
NM_005373.3(MPL):c.315T>C (p.Phe105=)
NM_005373.3(MPL):c.318G>A (p.Pro106=) rs370001905
NM_005373.3(MPL):c.333G>A (p.Val111=)
NM_005373.3(MPL):c.391+7G>A
NM_005373.3(MPL):c.392-9T>C
NM_005373.3(MPL):c.408C>A (p.Pro136=)
NM_005373.3(MPL):c.408C>G (p.Pro136=)
NM_005373.3(MPL):c.420G>A (p.Lys140=)
NM_005373.3(MPL):c.423C>T (p.Ala141=)
NM_005373.3(MPL):c.468G>A (p.Glu156=)
NM_005373.3(MPL):c.492C>T (p.Phe164=)
NM_005373.3(MPL):c.501C>T (p.Tyr167=)
NM_005373.3(MPL):c.513T>C (p.Tyr171=)
NM_005373.3(MPL):c.531G>A (p.Lys177=)
NM_005373.3(MPL):c.534C>T (p.Asn178=)
NM_005373.3(MPL):c.540T>C (p.Thr180=)
NM_005373.3(MPL):c.561G>A (p.Leu187=) rs1570465392
NM_005373.3(MPL):c.579C>T (p.Cys193=)
NM_005373.3(MPL):c.723C>T (p.Cys241=)
NM_005373.3(MPL):c.768G>A (p.Leu256=) rs1570465882
NM_005373.3(MPL):c.774C>T (p.Ser258=) rs746721066
NM_005373.3(MPL):c.79+7T>C
NM_005373.3(MPL):c.795C>T (p.Leu265=)
NM_005373.3(MPL):c.80-7T>C
NM_005373.3(MPL):c.921C>T (p.Asp307=)
NM_005373.3(MPL):c.933C>T (p.Ser311=)
NM_005373.3(MPL):c.936A>G (p.Gln312=)
NM_005373.3(MPL):c.963G>T (p.Arg321=) rs138636505
NM_005373.3(MPL):c.972C>T (p.Pro324=)
NM_005373.3(MPL):c.978C>T (p.Asp326=)
NM_005373.3(MPL):c.984C>T (p.Tyr328=)
NM_005373.3(MPL):c.987C>A (p.Pro329=)
NM_005373.3(MPL):c.999C>T (p.Asn333=)

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