ClinVar Miner

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

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_001048171.1(MUTYH):c.1076C>T (p.Ala359Val) rs35352891
NM_001048171.1(MUTYH):c.1104C>T (p.Ala368=) rs778193554
NM_001048171.1(MUTYH):c.1144+9A>T rs587780742
NM_001048171.1(MUTYH):c.1269G>A (p.Arg423=) rs199575659
NM_001048171.1(MUTYH):c.1353A>C (p.Pro451=) rs768239149
NM_001048171.1(MUTYH):c.1435-17C>G rs199664013
NM_001048171.1(MUTYH):c.1477-9T>C rs372815910
NM_001048171.1(MUTYH):c.174G>A (p.Pro58=) rs144551668
NM_001048171.1(MUTYH):c.180G>A (p.Glu60=) rs376861118
NM_001048171.1(MUTYH):c.324C>T (p.Asp108=) rs876660505
NM_001048171.1(MUTYH):c.330C>T (p.Asp110=) rs730881836
NM_001048171.1(MUTYH):c.347-7C>A rs863224698
NM_001048171.1(MUTYH):c.369G>A (p.Leu123=) rs1057517458
NM_001048171.1(MUTYH):c.37-7G>A rs780029247
NM_001048171.1(MUTYH):c.42C>T (p.Ile14=) rs202240122
NM_001048171.1(MUTYH):c.462+16G>A rs576152721
NM_001048171.1(MUTYH):c.483T>C (p.Ala161=) rs786201352
NM_001048171.1(MUTYH):c.534+20G>A rs776504435
NM_001048171.1(MUTYH):c.63C>T (p.Ala21=) rs201982344
NM_001048171.1(MUTYH):c.654C>T (p.Thr218=) rs780747266
NM_001048171.1(MUTYH):c.672C>T (p.Asn224=) rs767327888
NM_001048171.1(MUTYH):c.771C>T (p.Asp257=) rs730881838
NM_001048171.1(MUTYH):c.840C>T (p.Arg280=) rs587780750
NM_001048171.1(MUTYH):c.844C>T (p.Leu282=) rs778782508
NM_001048171.1(MUTYH):c.942C>T (p.Asp314=) rs587780752
NM_001048171.1(MUTYH):c.956-21T>C rs780013757
NM_001048171.1(MUTYH):c.956-27G>A rs188830619
NM_001048171.1(MUTYH):c.956-8G>A rs757672024
NM_012222.2(MUTYH):c.129C>T (p.Asn43=) rs141679570

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