List of variants in gene MUTYH reported as likely benign by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1103-27C>T	rs3219490	0.00300
NM_001048174.2(MUTYH):c.1501C>A (p.Leu501Met)	rs3219496	0.00154
NM_001128425.2(MUTYH):c.36+214G>C	rs568514678	0.00096
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys)	rs150792276	0.00081
NM_001048174.2(MUTYH):c.1424G>A (p.Gly475Glu)	rs3219494	0.00076
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys)	rs138089183	0.00051
NM_001048174.2(MUTYH):c.914-9C>T	rs3219488	0.00045
NM_001048174.2(MUTYH):c.1102+9A>T	rs587780742	0.00018
NM_001048174.2(MUTYH):c.1034C>T (p.Ala345Val)	rs35352891	0.00011
NM_001048174.2(MUTYH):c.-6-7G>A	rs780029247	0.00010
NM_001128425.2(MUTYH):c.36+179G>T	rs1418696430	0.00003
NM_001128425.2(MUTYH):c.161G>A (p.Cys54Tyr)	rs560905645	0.00002
NM_001048174.2(MUTYH):c.1102+42_1102+43del	rs775033999	0.00001
NM_001048174.2(MUTYH):c.1227G>A (p.Arg409=)	rs199575659	0.00001
NM_001048174.2(MUTYH):c.1533T>C (p.Thr511=)	rs756708148	0.00001
NM_001048174.2(MUTYH):c.887C>T (p.Ser296Leu)	rs558173961	0.00001
NM_001048174.2(MUTYH):c.903G>C (p.Val301=)	rs749048388	0.00001
NM_001048174.2(MUTYH):c.607-18_607-17del	rs765157527

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