ClinVar Miner

Variants in gene CBL with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 14
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HGVS dbSNP
NM_005188.3(CBL):c.1443G>T (p.Pro481=) rs768111719
NM_005188.3(CBL):c.2036+9G>T rs142704935
NM_005188.3(CBL):c.2252-8T>C rs555179188
NM_005188.4(CBL):c.107ACC[6] (p.His42del) rs373212940
NM_005188.4(CBL):c.107ACC[8] (p.His42dup) rs373212940
NM_005188.4(CBL):c.1227+4C>T rs201747825
NM_005188.4(CBL):c.1228-10dup rs397517078
NM_005188.4(CBL):c.12C>T (p.Asn4=) rs371567712
NM_005188.4(CBL):c.1359A>C (p.Pro453=) rs34732429
NM_005188.4(CBL):c.1641T>C (p.Pro547=) rs61755280
NM_005188.4(CBL):c.2190G>C (p.Thr730=) rs143840974
NM_005188.4(CBL):c.2269G>A (p.Ala757Thr) rs146517083
NM_005188.4(CBL):c.2345C>T (p.Pro782Leu) rs2229073
NM_005188.4(CBL):c.2710G>A (p.Val904Ile) rs17122769

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