ClinVar Miner

List of variants in gene MYH11 reported as uncertain significance for not specified

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_002474.3(MYH11):c.1749+4C>G rs776271431 0.00015
NM_002474.3(MYH11):c.3530C>T (p.Thr1177Met) rs201391947 0.00011
NM_002474.3(MYH11):c.3293+5C>T rs766421052 0.00008
NM_002474.3(MYH11):c.1913C>T (p.Ser638Leu) rs771128441 0.00006
NM_002474.3(MYH11):c.3858+13C>T rs375738696 0.00006
NM_002474.3(MYH11):c.1768G>A (p.Ala590Thr) rs745516001 0.00004
NM_002474.3(MYH11):c.2579A>T (p.Glu860Val) rs373789068 0.00004
NM_002474.3(MYH11):c.2785G>T (p.Ala929Ser) rs906679954 0.00004
NM_002474.3(MYH11):c.301G>A (p.Val101Met) rs375159635 0.00004
NM_002474.3(MYH11):c.2237C>G (p.Ala746Gly) rs778651094 0.00003
NM_002474.3(MYH11):c.2659G>A (p.Glu887Lys) rs201387564 0.00003
NM_002474.3(MYH11):c.3214G>A (p.Ala1072Thr) rs759155353 0.00002
NM_002474.3(MYH11):c.1576-4A>G rs189193825 0.00001
NM_002474.3(MYH11):c.1864+8C>T rs1297078684 0.00001
NM_002474.3(MYH11):c.2098C>T (p.Arg700Trp) rs886038932 0.00001
NM_002474.3(MYH11):c.2297G>A (p.Ser766Asn) rs1050298581 0.00001
NM_002474.3(MYH11):c.2426G>A (p.Arg809Lys) rs534802983 0.00001
NM_002474.3(MYH11):c.2446A>C (p.Met816Leu) rs1243566183 0.00001
NM_002474.3(MYH11):c.2476T>C (p.Tyr826His) rs1436181127 0.00001
NM_002474.3(MYH11):c.3124C>T (p.Arg1042Trp) rs774490005 0.00001
NM_002474.3(MYH11):c.3152A>G (p.Gln1051Arg) rs1555557294 0.00001
NM_002474.3(MYH11):c.3233T>C (p.Ile1078Thr) rs193922629 0.00001
NM_002474.3(MYH11):c.62T>C (p.Ile21Thr) rs777372840 0.00001
GRCh37/hg19 16p13.11(chr16:15869293-15907589)x1
NM_002474.3(MYH11):c.1202T>C (p.Ile401Thr) rs773998062
NM_002474.3(MYH11):c.1575+6G>A rs2041769693
NM_002474.3(MYH11):c.1864+18C>T
NM_002474.3(MYH11):c.2195C>A (p.Ala732Glu) rs764831521
NM_002474.3(MYH11):c.2666A>C (p.Lys889Thr) rs1057518502
NM_002474.3(MYH11):c.2747A>G (p.Lys916Arg) rs1382626826
NM_002474.3(MYH11):c.3115C>G (p.Leu1039Val) rs1223757069
NM_002474.3(MYH11):c.3541_3542delinsGC (p.Lys1181Ala) rs1555555783
NM_002474.3(MYH11):c.3654C>G (p.Ala1218=) rs1555554196
NM_002474.3(MYH11):c.3778C>T (p.Gln1260Ter) rs1060499879
NM_002474.3(MYH11):c.3781G>A (p.Val1261Met) rs1057518389
NM_002474.3(MYH11):c.404C>T (p.Ser135Leu) rs760445629
NM_002474.3(MYH11):c.531-19_531-17del rs2042478963
NM_002474.3(MYH11):c.809G>C (p.Arg270Pro)
NM_002474.3(MYH11):c.886A>G (p.Arg296Gly) rs2042214133
NM_002474.3(MYH11):c.95C>G (p.Ala32Gly)

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