"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 719810	NM_005157.6(ABL1):c.249T>G (p.Thr83=)	ABL1	Single nucleotide variant (synonymous variant)	Congenital heart defects and skeletal malformations syndrome +2 more	GBenign/Likely benign
Select item 133450	NM_005157.6(ABL1):c.740A>G (p.Lys247Arg)	ABL1 (K247R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 713869	NM_005157.6(ABL1):c.1899C>T (p.Ala633=)	ABL1	Single nucleotide variant (synonymous variant)	Chronic myelogenous leukemia, BCR-ABL1 positive +2 more	GBenign/Likely benign
Select item 731278	NM_005157.6(ABL1):c.2040C>T (p.Gly680=)	ABL1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 133445	NM_005157.6(ABL1):c.2116G>A (p.Gly706Ser)	ABL1 (G706S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1299786	NM_005157.6(ABL1):c.2205G>A (p.Thr735=)	ABL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 781935	NM_005157.6(ABL1):c.2916G>A (p.Ser972=)	ABL1	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar