BCL2L1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1050523	NC_000020.11:g.31659579dup	BCL2L1	Duplication	not provided	GUncertain significance
Select item 1049032	NC_000020.11:g.31661977T>G	BCL2L1	Single nucleotide variant	not provided	GUncertain significance
Select item 1050585	NC_000020.11:g.31663046_31663056AT[6]AC[4]AT[4]ACATATAT[2]ATACACACACATATACACACACACACACACACACATATATATATA[1]	BCL2L1	Microsatellite	not provided	GUncertain significance
Select item 981886	NM_138578.3(BCL2L1):c.674T>C (p.Leu225Pro)	BCL2L1 (L162P +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 3133391	NM_138578.3(BCL2L1):c.626G>A (p.Arg209His)	BCL2L1 (R209H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277993	NM_138578.3(BCL2L1):c.608G>A (p.Ser203Asn)	BCL2L1 (S140N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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