List of variants in gene combination MUTYH, TOE1 reported as uncertain significance for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_025077.4(TOE1):c.52+77G>A	rs3219466	0.02177
NM_025077.4(TOE1):c.106G>A (p.Val36Ile)	rs140393352	0.00065
NM_001128425.2(MUTYH):c.17C>A (p.Ser6Tyr)	rs587782837	0.00002
NM_025077.4(TOE1):c.-37T>A	rs759654665	0.00001
NM_025077.4(TOE1):c.-38G>C	rs774530388	0.00001
NM_025077.4(TOE1):c.1A>G (p.Met1Val)	rs865954220	0.00001
NM_025077.4(TOE1):c.6C>T (p.Ala2=)	rs876659248	0.00001
NM_001128425.2(MUTYH):c.17C>G (p.Ser6Cys)	rs587782837
NM_001128425.2(MUTYH):c.32T>G (p.Leu11Arg)	rs752665489
NM_025077.4(TOE1):c.-38dup	rs1557517901
NM_025077.4(TOE1):c.-54G>T	rs540793556
NM_025077.4(TOE1):c.4G>A (p.Ala2Thr)
NM_025077.4(TOE1):c.4G>C (p.Ala2Pro)	rs781609463
NM_025077.4(TOE1):c.8C>A (p.Ala3Asp)

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