List of variants in gene MUTYH reported as benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.930G>C (p.Gln310His)	rs3219489	0.26909
NM_001048174.2(MUTYH):c.22G>A (p.Val8Met)	rs3219484	0.04691
NM_001048174.2(MUTYH):c.1517G>A (p.Arg506Gln)	rs3219497	0.01036
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.421-4A>G	rs201678305	0.00496
NM_001048174.2(MUTYH):c.1501C>A (p.Leu501Met)	rs3219496	0.00153
NM_001048174.2(MUTYH):c.11C>T (p.Pro4Leu)	rs79777494	0.00044
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp)	rs75321043	0.00044
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met)	rs144079536	0.00041
NM_001048174.2(MUTYH):c.1392+2C>T	rs140288388	0.00031
NM_001048174.2(MUTYH):c.1171G>A (p.Ala391Thr)	rs587780744	0.00010
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=)	rs121908380

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