ClinVar Miner

List of variants in gene combination CBL, MCAM reported as uncertain significance for Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia

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Total variants: 39
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HGVS dbSNP
NM_005188.3(CBL):c.*5986T>C rs764329156
NM_005188.3(CBL):c.*6099A>G rs575606651
NM_005188.3(CBL):c.*6126T>A rs886047803
NM_005188.3(CBL):c.*6175A>G rs775450592
NM_005188.3(CBL):c.*6265C>A rs886047804
NM_005188.3(CBL):c.*6362G>A rs886047805
NM_005188.3(CBL):c.*6430G>C rs886047806
NM_005188.3(CBL):c.*6575G>C rs569180524
NM_005188.3(CBL):c.*6703T>C rs562568416
NM_005188.3(CBL):c.*6767C>G rs539341635
NM_005188.3(CBL):c.*6933C>A rs886047807
NM_005188.3(CBL):c.*6980T>C rs886047808
NM_005188.3(CBL):c.*7081T>G rs886047809
NM_005188.3(CBL):c.*7167A>C rs886047812
NM_005188.3(CBL):c.*7659C>A rs567049953
NM_005188.3(CBL):c.*7659C>G rs567049953
NM_005188.3(CBL):c.*7689C>G rs187961956
NM_005188.3(CBL):c.*7761G>A rs745412309
NM_005188.3(CBL):c.*7904G>A rs886047813
NM_005188.3(CBL):c.*8058C>T rs569107221
NM_005188.4(CBL):c.*6261A>T
NM_005188.4(CBL):c.*6429T>C
NM_005188.4(CBL):c.*6484G>A
NM_005188.4(CBL):c.*6528T>C
NM_005188.4(CBL):c.*6532A>G
NM_005188.4(CBL):c.*6678G>A
NM_005188.4(CBL):c.*6712C>G
NM_005188.4(CBL):c.*6729C>T
NM_005188.4(CBL):c.*6795A>G
NM_005188.4(CBL):c.*6806T>C
NM_005188.4(CBL):c.*6872A>T
NM_005188.4(CBL):c.*7030T>G
NM_005188.4(CBL):c.*7241A>G
NM_005188.4(CBL):c.*7601G>A
NM_005188.4(CBL):c.*7659C>T
NM_005188.4(CBL):c.*7855C>T
NM_005188.4(CBL):c.*7878C>T
NM_005188.4(CBL):c.*7924C>A
NM_005188.4(CBL):c.*8318C>T

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