ClinVar Miner

List of variants in gene MYO6 reported as uncertain significance for not specified

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_004999.4(MYO6):c.3529C>T (p.Arg1177Cys) rs146419641 0.00069
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys) rs141845119 0.00039
NM_004999.4(MYO6):c.52A>G (p.Met18Val) rs142516093 0.00030
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys) rs201507590 0.00026
NM_004999.4(MYO6):c.3176G>C (p.Arg1059Thr) rs202214380 0.00020
NM_004999.4(MYO6):c.2472T>G (p.Ile824Met) rs368132510 0.00014
NM_004999.4(MYO6):c.2616G>T (p.Lys872Asn) rs139542573 0.00012
NM_004999.4(MYO6):c.1748C>T (p.Ala583Val) rs766684928 0.00006
NM_004999.4(MYO6):c.2818C>T (p.Arg940Cys) rs200205409 0.00006
NM_004999.4(MYO6):c.3367A>G (p.Asn1123Asp) rs189411232 0.00006
NM_004999.4(MYO6):c.2552A>C (p.Asp851Ala) rs142423106 0.00003
NM_004999.4(MYO6):c.2716T>C (p.Ser906Pro) rs727505048 0.00003
NM_004999.4(MYO6):c.3236A>G (p.Lys1079Arg) rs753378509 0.00003
NM_004999.4(MYO6):c.3386G>A (p.Arg1129His) rs779885818 0.00003
NM_004999.4(MYO6):c.3679T>C (p.Cys1227Arg) rs370061746 0.00003
NM_004999.4(MYO6):c.217C>G (p.Leu73Val) rs759372006 0.00002
NM_004999.4(MYO6):c.2926G>T (p.Asp976Tyr) rs201168408 0.00002
NM_004999.4(MYO6):c.3505C>T (p.Arg1169Cys) rs144006872 0.00002
NM_004999.4(MYO6):c.1079-5A>G rs774020683 0.00001
NM_004999.4(MYO6):c.178G>C (p.Glu60Gln) rs757420692 0.00001
NM_004999.4(MYO6):c.1853G>A (p.Arg618Gln) rs777201018 0.00001
NM_004999.4(MYO6):c.2507G>A (p.Arg836His) rs876657909 0.00001
NM_004999.4(MYO6):c.2837G>A (p.Arg946His) rs781754117 0.00001
NM_004999.4(MYO6):c.3137+5G>A rs397517050 0.00001
NM_004999.4(MYO6):c.647A>T (p.Glu216Val) rs121912559 0.00001
NM_004999.4(MYO6):c.1250A>G (p.Asn417Ser) rs1554210769
NM_004999.4(MYO6):c.1264G>A (p.Ala422Thr) rs1583287198
NM_004999.4(MYO6):c.1516G>T (p.Val506Leu) rs1554211583
NM_004999.4(MYO6):c.1837A>G (p.Arg613Gly) rs781019390
NM_004999.4(MYO6):c.1881CAA[1] (p.Asn628del) rs1233700794
NM_004999.4(MYO6):c.2107G>C (p.Gly703Arg) rs753163582
NM_004999.4(MYO6):c.2266G>A (p.Val756Ile) rs864309590
NM_004999.4(MYO6):c.2548C>G (p.Leu850Val) rs397517047
NM_004999.4(MYO6):c.2562T>A (p.Asn854Lys) rs1583365903
NM_004999.4(MYO6):c.2751dup (p.Gln918fs) rs551348450
NM_004999.4(MYO6):c.2779A>G (p.Arg927Gly) rs986223790
NM_004999.4(MYO6):c.2898AGA[3] (p.Glu970del) rs727504743
NM_004999.4(MYO6):c.2911A>G (p.Arg971Gly) rs397517049
NM_004999.4(MYO6):c.292A>G (p.Asn98Asp) rs876657910
NM_004999.4(MYO6):c.3198C>T (p.Thr1066=) rs143864052
NM_004999.4(MYO6):c.3326T>C (p.Leu1109Pro) rs1554222430
NM_004999.4(MYO6):c.3391C>T (p.Pro1131Ser) rs727503327
NM_004999.4(MYO6):c.3610C>T (p.Arg1204Trp) rs876657911
NM_004999.4(MYO6):c.3644T>C (p.Ile1215Thr) rs1554223853
NM_004999.4(MYO6):c.3646C>G (p.Leu1216Val) rs876657908
NM_004999.4(MYO6):c.3833C>T (p.Ala1278Val) rs397517052
NM_004999.4(MYO6):c.470A>G (p.Lys157Arg) rs397517053
NM_004999.4(MYO6):c.558C>A (p.Asn186Lys) rs397517054

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