List of variants in gene CBL reported as uncertain significance for Noonan-like syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_005188.4(CBL):c.2414_2416dup (p.Leu805_Asp806insVal)	rs777761446	0.00001
NM_005188.4(CBL):c.*1732del	rs549459958
NM_005188.4(CBL):c.*2129dup	rs886047782
NM_005188.4(CBL):c.*2762dup	rs886047785
NM_005188.4(CBL):c.*3106del	rs886047787
NM_005188.4(CBL):c.*4863dup	rs572265582
NM_005188.4(CBL):c.559_560insCAA	rs3833768
NM_005188.4(CBL):c.*5771T>A	rs886047800
NM_005188.4(CBL):c.7170_7173del	rs112360309
NM_005188.4(CBL):c.*7173del	rs112360309
NM_005188.4(CBL):c.8164_8167del	rs886047814
NM_005188.4(CBL):c.686A>T (p.Asp229Val)	rs1414848678

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