List of variants in gene MUTYH reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.-7+5C>G	rs3219468	0.98714
NM_001048174.2(MUTYH):c.420+35A>G	rs3219487	0.93920
NM_001048174.2(MUTYH):c.1393-40C>G	rs3219493	0.93580
NM_001048174.2(MUTYH):c.930G>C (p.Gln310His)	rs3219489	0.26909
NM_001048174.2(MUTYH):c.-7+1521G>A	rs3219472	0.26253
NM_001048174.2(MUTYH):c.-7+1144C>A	rs74688071	0.20081
NM_001048174.2(MUTYH):c.1393-125C>A	rs3219492	0.12754
NM_001048174.2(MUTYH):c.1434+73C>T	rs3219495	0.06702
NM_001048174.2(MUTYH):c.22G>A (p.Val8Met)	rs3219484	0.04691
NM_001048174.2(MUTYH):c.115+151G>A	rs3219486	0.03415
NM_001048174.2(MUTYH):c.115+30A>G	rs3219485	0.02245
NM_001048174.2(MUTYH):c.1517G>A (p.Arg506Gln)	rs3219497	0.01036
NM_001048174.2(MUTYH):c.-7+1625C>T	rs3219473	0.01008
NM_001048174.2(MUTYH):c.1460C>T (p.Ser487Phe)	rs140118273	0.00973
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=)	rs74318065	0.00596
NM_001048174.2(MUTYH):c.1501C>A (p.Leu501Met)	rs3219496	0.00153
NM_001048174.2(MUTYH):c.1393-28G>A	rs373226007	0.00061
NM_001048174.2(MUTYH):c.1365C>T (p.Thr455=)	rs150269172	0.00043
NM_001048174.2(MUTYH):c.-6-7G>A	rs780029247	0.00013
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val)	rs200872702	0.00010
NM_001048174.2(MUTYH):c.1351G>A (p.Glu451Lys)	rs376790729	0.00006
NM_001048174.2(MUTYH):c.796C>T (p.Arg266Cys)	rs199840380	0.00002
NM_001048174.2(MUTYH):c.116-55C>T	rs1316542179	0.00001
NM_001048174.2(MUTYH):c.1209C>G (p.Leu403=)	rs577542506
NM_001048174.2(MUTYH):c.294G>T (p.Arg98=)	rs1232031176

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