ClinVar Miner

List of variants in gene MUTYH reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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Total variants: 24
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HGVS dbSNP gnomAD frequency
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.850-2A>G rs77542170 0.00035
NM_001048174.2(MUTYH):c.737G>A (p.Arg246Gln) rs149866955 0.00023
NM_001048174.2(MUTYH):c.848G>A (p.Arg283Lys) rs149342980 0.00021
NM_001048174.2(MUTYH):c.1483C>T (p.Arg495Cys) rs147480076 0.00016
NM_001048174.2(MUTYH):c.616G>A (p.Val206Met) rs200165598 0.00016
NM_001048174.2(MUTYH):c.397G>C (p.Asp133His) rs564930066 0.00010
NM_001048174.2(MUTYH):c.1333G>A (p.Ala445Thr) rs192816572 0.00008
NM_001048174.2(MUTYH):c.1504G>T (p.Asp502Tyr) rs147923905 0.00008
NM_001048174.2(MUTYH):c.1381G>A (p.Ala461Thr) rs587782263 0.00006
NM_001048174.2(MUTYH):c.1007G>A (p.Arg336His) rs587780741 0.00003
NM_001048174.2(MUTYH):c.439G>T (p.Ala147Ser) rs770478980 0.00002
NM_001048174.2(MUTYH):c.1015C>G (p.Pro339Ala) rs876660262 0.00001
NM_001048174.2(MUTYH):c.409G>A (p.Ala137Thr) rs201103359 0.00001
NM_001048174.2(MUTYH):c.512G>A (p.Gly171Asp) rs1263648272 0.00001
NM_001048174.2(MUTYH):c.595G>A (p.Ala199Thr) rs369854269 0.00001
NM_001048174.2(MUTYH):c.683C>T (p.Thr228Ile) rs766173546 0.00001
NM_001048174.2(MUTYH):c.986A>G (p.Asn329Ser) rs754178539 0.00001
NM_001048174.2(MUTYH):c.1069G>T (p.Ala357Ser) rs876659232
NM_001048174.2(MUTYH):c.1196G>T (p.Trp399Leu) rs876658787
NM_001048174.2(MUTYH):c.407G>A (p.Ser136Asn) rs1557480827
NM_001048174.2(MUTYH):c.459T>G (p.Ser153=)
NM_001048174.2(MUTYH):c.814T>C (p.Cys272Arg)

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