ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by Mendelics

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Total variants: 70
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HGVS dbSNP
NM_000179.2(MSH6):c.1054G>A (p.Val352Ile) rs730881787
NM_000179.2(MSH6):c.107C>T (p.Ala36Val) rs61756469
NM_000179.2(MSH6):c.1120A>G (p.Lys374Glu) rs1558660575
NM_000179.2(MSH6):c.1127A>G (p.Glu376Gly) rs764150912
NM_000179.2(MSH6):c.1190A>G (p.Tyr397Cys) rs63750065
NM_000179.2(MSH6):c.1321C>G (p.Leu441Val) rs1553412749
NM_000179.2(MSH6):c.1406A>G (p.Tyr469Cys) rs748165218
NM_000179.2(MSH6):c.1651G>A (p.Gly551Ser) rs1558662449
NM_000179.2(MSH6):c.1661G>A (p.Arg554His) rs730881791
NM_000179.2(MSH6):c.1729C>T (p.Arg577Cys) rs542838372
NM_000179.2(MSH6):c.1730G>A (p.Arg577His) rs376220212
NM_000179.2(MSH6):c.175C>A (p.Pro59Thr) rs761033647
NM_000179.2(MSH6):c.1814C>G (p.Thr605Ser) rs587781616
NM_000179.2(MSH6):c.1844G>C (p.Cys615Ser) rs730881793
NM_000179.2(MSH6):c.1932G>C (p.Arg644Ser) rs34938432
NM_000179.2(MSH6):c.2107A>G (p.Met703Val) rs751867550
NM_000179.2(MSH6):c.2161A>G (p.Arg721Gly) rs537604099
NM_000179.2(MSH6):c.2180C>T (p.Thr727Ile)
NM_000179.2(MSH6):c.2347T>A (p.Cys783Ser) rs373721483
NM_000179.2(MSH6):c.2408A>G (p.Asp803Gly) rs63751450
NM_000179.2(MSH6):c.2419G>A (p.Glu807Lys) rs587779923
NM_000179.2(MSH6):c.2480A>C (p.Asn827Thr) rs1558665569
NM_000179.2(MSH6):c.2629G>A (p.Glu877Lys) rs730881797
NM_000179.2(MSH6):c.2640_2641insAAA (p.Gly881_Phe882insLys) rs1252374906
NM_000179.2(MSH6):c.2667G>T (p.Gln889His) rs149945495
NM_000179.2(MSH6):c.2693C>G (p.Pro898Arg) rs876661281
NM_000179.2(MSH6):c.2732G>A (p.Arg911Gln) rs761622304
NM_000179.2(MSH6):c.2752C>T (p.His918Tyr) rs1558666591
NM_000179.2(MSH6):c.275C>T (p.Pro92Leu) rs1257646433
NM_000179.2(MSH6):c.2963G>T (p.Arg988Leu) rs115386788
NM_000179.2(MSH6):c.3019T>C (p.Trp1007Arg) rs1553414398
NM_000179.2(MSH6):c.3100C>T (p.Arg1034Trp) rs587779930
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3245C>T (p.Pro1082Leu) rs191109849
NM_000179.2(MSH6):c.3260C>G (p.Pro1087Arg) rs63750753
NM_000179.2(MSH6):c.3270G>C (p.Glu1090Asp) rs876660165
NM_000179.2(MSH6):c.3307T>G (p.Phe1103Val) rs1553331522
NM_000179.2(MSH6):c.334A>G (p.Asn112Asp) rs864622397
NM_000179.2(MSH6):c.3452C>G (p.Ala1151Gly) rs587782625
NM_000179.2(MSH6):c.3478G>A (p.Val1160Ile) rs376799914
NM_000179.2(MSH6):c.34C>A (p.Pro12Thr) rs587782084
NM_000179.2(MSH6):c.3524C>G (p.Thr1175Ser) rs369583604
NM_000179.2(MSH6):c.3598A>G (p.Ile1200Val) rs781627838
NM_000179.2(MSH6):c.359T>C (p.Ile120Thr) rs775971872
NM_000179.2(MSH6):c.3613_3615dup (p.Thr1205dup) rs1558390840
NM_000179.2(MSH6):c.3636G>T (p.Val1212=) rs1363247790
NM_000179.2(MSH6):c.3841G>C (p.Glu1281Gln) rs876659115
NM_000179.2(MSH6):c.3847A>G (p.Ile1283Val) rs144714869
NM_000179.2(MSH6):c.3904G>A (p.Ala1302Thr) rs1553333561
NM_000179.2(MSH6):c.3936T>C (p.Val1312=) rs61753796
NM_000179.2(MSH6):c.3961A>G (p.Arg1321Gly) rs41295278
NM_000179.2(MSH6):c.3986C>T (p.Ser1329Leu) rs199594809
NM_000179.2(MSH6):c.4001+11_4001+15dupAACTA rs587779302
NM_000179.2(MSH6):c.4001+27TAAC[3] rs267608136
NM_000179.2(MSH6):c.4001+42_4001+44dup rs926031657
NM_000179.2(MSH6):c.4002-10T>A rs545466048
NM_000179.2(MSH6):c.4002-4T>C rs370428032
NM_000179.2(MSH6):c.4004A>C (p.Glu1335Ala) rs564434147
NM_000179.2(MSH6):c.4022_4077dup (p.Leu1360delinsLysGlyGlnLeuTer) rs1553334006
NM_000179.2(MSH6):c.4034_4042del (p.Val1345_Ala1347del) rs864622703
NM_000179.2(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer) rs55740729
NM_000179.2(MSH6):c.545C>G (p.Ala182Gly)
NM_000179.2(MSH6):c.627+26_627+37del rs1558656848
NM_000179.2(MSH6):c.650A>G (p.Asp217Gly) rs554012110
NM_000179.2(MSH6):c.663A>C (p.Glu221Asp) rs41557217
NM_000179.2(MSH6):c.818G>T (p.Gly273Val) rs769610487
NM_000179.2(MSH6):c.838A>G (p.Ser280Gly) rs1558659442
NM_000179.2(MSH6):c.905G>C (p.Arg302Thr) rs587781510
NM_000179.2(MSH6):c.923G>C (p.Gly308Ala) rs1553412354
NM_000179.2(MSH6):c.998C>T (p.Thr333Ile) rs587781983

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