List of variants in gene MUTYH reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.304+56G>A	rs201858839	0.00274
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys)	rs138089183	0.00051
NM_001048174.2(MUTYH):c.1034C>T (p.Ala345Val)	rs35352891	0.00011
NM_001048174.2(MUTYH):c.1400G>A (p.Arg467His)	rs144111588	0.00008
NM_001048174.2(MUTYH):c.729C>T (p.Asp243=)	rs730881838	0.00006
NM_001048174.2(MUTYH):c.366C>T (p.Thr122=)	rs368383907	0.00003
NM_001048174.2(MUTYH):c.1194T>C (p.Arg398=)	rs777361121	0.00001
NM_001048174.2(MUTYH):c.1320C>T (p.Thr440=)	rs746668146	0.00001
NM_001048174.2(MUTYH):c.288C>T (p.Asp96=)	rs730881836	0.00001
NM_001048174.2(MUTYH):c.802C>T (p.Leu268=)	rs778782508	0.00001
NM_001048174.2(MUTYH):c.1413C>T (p.Gly471=)
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=)	rs121908380
NM_001048174.2(MUTYH):c.606+21C>A	rs148552450
NM_001048174.2(MUTYH):c.645G>A (p.Leu215=)	rs1060504204
NM_001048174.2(MUTYH):c.774G>A (p.Gly258=)	rs771290019

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