Related gene-specific medical variations for Gene (Select 25936) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2519969	NM_015471.4(NSL1):c.13C>T (p.Pro5Ser)	LOC129932483, NSL1 (P5S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2395838	NM_015471.4(NSL1):c.7G>A (p.Gly3Arg)	LOC129932483, NSL1 (G3R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313000	NM_015471.4(NSL1):c.38C>A (p.Pro13Gln)	LOC129932483, NSL1 (P13Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783965	NM_015471.4(NSL1):c.39A>G (p.Pro13=)	LOC129932483, NSL1	Single nucleotide variant (synonymous variant)	not provided	GBenign

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