Related gene-specific medical variations for Gene (Select 101928020) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2550007	NM_152519.4(KANSL1L):c.2030T>C (p.Val677Ala)	KANSL1L, KANSL1L-AS1 (V677A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547551	NM_152519.4(KANSL1L):c.1830T>A (p.Ser610Arg)	KANSL1L, KANSL1L-AS1 (S610R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513892	NM_152519.4(KANSL1L):c.2050T>C (p.Trp684Arg)	KANSL1L, KANSL1L-AS1 (W684R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310028	NM_152519.4(KANSL1L):c.1799T>A (p.Met600Lys)	KANSL1L, KANSL1L-AS1 (M600K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277372	NM_152519.4(KANSL1L):c.2119G>A (p.Gly707Arg)	KANSL1L, KANSL1L-AS1 (G707R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 735231	NM_152519.4(KANSL1L):c.2040T>C (p.Thr680=)	KANSL1L, KANSL1L-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

ClinVar