List of variants reported as uncertain significance for Lynch syndrome 5 by Mendelics

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.1932G>C (p.Arg644Ser)	rs34938432	0.00037
NM_000179.3(MSH6):c.3961A>G (p.Arg1321Gly)	rs41295278	0.00019
NM_000179.3(MSH6):c.884A>G (p.Lys295Arg)	rs267608051	0.00014
NM_000179.3(MSH6):c.628-7C>A	rs373129248	0.00011
NM_000179.3(MSH6):c.3727A>T (p.Thr1243Ser)	rs147453999	0.00009
NM_000179.3(MSH6):c.2408A>G (p.Asp803Gly)	rs63751450	0.00004
NM_000179.3(MSH6):c.4004A>C (p.Glu1335Ala)	rs564434147	0.00004
NM_000179.3(MSH6):c.1696G>A (p.Gly566Arg)	rs63749973	0.00003
NM_000179.3(MSH6):c.359T>C (p.Ile120Thr)	rs775971872	0.00003
NM_000179.3(MSH6):c.532C>T (p.Arg178Cys)	rs730881813	0.00003
NM_000179.3(MSH6):c.3851C>T (p.Thr1284Met)	rs63750836	0.00002
NM_000179.3(MSH6):c.2107A>G (p.Met703Val)	rs751867550	0.00001
NM_000179.3(MSH6):c.2629G>A (p.Glu877Lys)	rs730881797	0.00001
NM_000179.3(MSH6):c.533G>A (p.Arg178His)	rs786204186	0.00001
NM_000179.3(MSH6):c.998C>T (p.Thr333Ile)	rs587781983	0.00001
NM_000179.3(MSH6):c.1508C>T (p.Ser503Phe)	rs63750897
NM_000179.3(MSH6):c.175C>A (p.Pro59Thr)	rs761033647
NM_000179.3(MSH6):c.2298T>G (p.His766Gln)	rs768535330
NM_000179.3(MSH6):c.2479A>G (p.Asn827Asp)	rs878853716
NM_000179.3(MSH6):c.253C>T (p.Pro85Ser)	rs779664343
NM_000179.3(MSH6):c.2752C>T (p.His918Tyr)	rs1558666591
NM_000179.3(MSH6):c.3314G>T (p.Gly1105Val)	rs1060502910
NM_000179.3(MSH6):c.34C>A (p.Pro12Thr)	rs587782084
NM_000179.3(MSH6):c.3971AGA[1] (p.Lys1325del)	rs587779300
NM_000179.3(MSH6):c.3992G>A (p.Arg1331Gln)	rs184131049
NM_000179.3(MSH6):c.4034_4042del (p.Val1345_Ala1347del)	rs864622703
NM_000179.3(MSH6):c.627+26_627+37del	rs1558656848
NM_000179.3(MSH6):c.838A>G (p.Ser280Gly)	rs1558659442
NM_000179.3(MSH6):c.905G>C (p.Arg302Thr)	rs587781510
NM_001190274.2(FBXO11):c.*906G>T	rs1572751620
NM_001190274.2(FBXO11):c.1076A>G (p.Asn359Ser)	rs1572806551

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