Related gene-specific medical variations for Gene (Select 11097) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3203201	NM_007342.3(NUP42):c.74C>T (p.Ala25Val)	LOC129998064, NUP42 (A25V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3203200	NM_007342.3(NUP42):c.73G>A (p.Ala25Thr)	LOC129998064, NUP42 (A25T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3203197	NM_007342.3(NUP42):c.4G>A (p.Ala2Thr)	LOC129998064, NUP42 (A2T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3203196	NM_007342.3(NUP42):c.43G>A (p.Gly15Arg)	LOC129998064, NUP42 (G15R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3203195	NM_007342.3(NUP42):c.37C>A (p.Arg13Ser)	LOC129998064, NUP42 (R13S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462207	NM_007342.3(NUP42):c.7A>G (p.Ile3Val)	LOC129998064, NUP42 (I3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar