ClinVar Miner

List of variants in gene MSH6 reported as likely benign by University of Washington Department of Laboratory Medicine,University of Washington

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Gene type:
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Total variants: 34
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HGVS dbSNP
NM_000179.2(MSH6):c.1021T>G (p.Ser341Ala) rs1558660119
NM_000179.2(MSH6):c.1081C>T (p.Arg361Cys) rs587782651
NM_000179.2(MSH6):c.1168G>A (p.Asp390Asn) rs147737737
NM_000179.2(MSH6):c.1207C>A (p.Leu403Ile) rs876659223
NM_000179.2(MSH6):c.133G>T (p.Gly45Cys) rs978968846
NM_000179.2(MSH6):c.1400G>A (p.Gly467Asp) rs1558661547
NM_000179.2(MSH6):c.1822A>G (p.Ile608Val) rs201613780
NM_000179.2(MSH6):c.1904G>A (p.Arg635Lys) rs1558663439
NM_000179.2(MSH6):c.260+265G>A rs3136231
NM_000179.2(MSH6):c.260+279C>T rs869312601
NM_000179.2(MSH6):c.260+84T>G rs869312603
NM_000179.2(MSH6):c.261-14C>T rs369366445
NM_000179.2(MSH6):c.261-3611A>G rs528466684
NM_000179.2(MSH6):c.261-565C>T rs553631780
NM_000179.2(MSH6):c.3029C>T (p.Thr1010Ile) rs768925694
NM_000179.2(MSH6):c.3126A>C (p.Lys1042Asn) rs1558668218
NM_000179.2(MSH6):c.3172+875A>C rs187192537
NM_000179.2(MSH6):c.3173-18T>A rs189672273
NM_000179.2(MSH6):c.3300G>A (p.Thr1100=) rs540252208
NM_000179.2(MSH6):c.3426G>A (p.Thr1142=) rs747771350
NM_000179.2(MSH6):c.3557-40T>A rs189436849
NM_000179.2(MSH6):c.3801+5G>A rs201080919
NM_000179.2(MSH6):c.3964G>A (p.Glu1322Lys) rs1553333707
NM_000179.2(MSH6):c.4018A>G (p.Ser1340Gly) rs1558395603
NM_000179.2(MSH6):c.458-1174T>C rs869312602
NM_000179.2(MSH6):c.458-509G>A rs556222101
NM_000179.2(MSH6):c.458-518G>T rs869312600
NM_000179.2(MSH6):c.475G>A (p.Ala159Thr) rs1553411396
NM_000179.2(MSH6):c.511G>C (p.Glu171Gln) rs1558656518
NM_000179.2(MSH6):c.542A>C (p.Glu181Ala) rs1558656620
NM_000179.2(MSH6):c.627+267G>A rs772499816
NM_000179.2(MSH6):c.627+566T>G rs869312604
NM_000179.2(MSH6):c.911T>C (p.Val304Ala) rs1481054050
NM_000179.2(MSH6):c.971A>G (p.Lys324Arg) rs1558659961

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