List of variants in gene MSH6 reported as not provided for colorectal cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.650A>G (p.Asp217Gly)	rs554012110	0.00013
NM_000179.3(MSH6):c.1402C>T (p.Arg468Cys)	rs369456858	0.00004
NM_000179.3(MSH6):c.1097A>G (p.Tyr366Cys)	rs1482767334	0.00001
NM_000179.3(MSH6):c.1346T>C (p.Leu449Pro)	rs63750741	0.00001
NM_000179.3(MSH6):c.1565A>G (p.Gln522Arg)	rs63751009	0.00001
NM_000179.3(MSH6):c.467C>G (p.Ser156Ter)	rs63749873	0.00001
NM_000179.3(MSH6):c.651dup (p.Lys218Ter)	rs63750955	0.00001
NM_000179.3(MSH6):c.905G>A (p.Arg302Lys)	rs587781510	0.00001
NM_000179.3(MSH6):c.24_28del	rs587779200
NM_000179.3(MSH6):c.1190_1191del (p.Tyr397fs)	rs63750439
NM_000179.3(MSH6):c.1480G>T (p.Ala494Ser)	rs758699749
NM_000179.3(MSH6):c.1614_1615delinsAG (p.Tyr538_Leu539delinsTer)	rs267608049
NM_000179.3(MSH6):c.1645del (p.Ser549fs)	rs876661033
NM_000179.3(MSH6):c.2075A>G (p.Lys692Arg)	rs975991506
NM_000179.3(MSH6):c.2230dup (p.Glu744fs)	rs786201050
NM_000179.3(MSH6):c.2931C>G (p.Tyr977Ter)	rs63750111
NM_000179.3(MSH6):c.2983G>T (p.Glu995Ter)	rs63750258
NM_000179.3(MSH6):c.322T>C (p.Cys108Arg)	rs1668689651
NM_000179.3(MSH6):c.3261del (p.Phe1088fs)	rs267608078
NM_000179.3(MSH6):c.3439-1G>T	rs587779263
NM_000179.3(MSH6):c.3450A>C (p.Leu1150Phe)	rs762134820
NM_000179.3(MSH6):c.3768T>G (p.Tyr1256Ter)	rs63751058
NM_000179.3(MSH6):c.3848_3850dup (p.Ile1283dup)	rs1553333420
NM_000179.3(MSH6):c.3959_3962del (p.Ala1320fs)	rs267608120
NM_000179.3(MSH6):c.3984_3987dup (p.Leu1330fs)	rs267608121

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