Related gene-specific medical variations for Gene (Select 51299) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2569428	NM_016588.3(NRN1):c.391T>G (p.Ser131Ala)	LOC126859570, NRN1 (S131A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569427	NM_016588.3(NRN1):c.373T>C (p.Phe125Leu)	LOC126859570, NRN1 (F125L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2357664	NM_016588.3(NRN1):c.375C>G (p.Phe125Leu)	LOC126859570, NRN1 (F125L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2291645	NM_016588.3(NRN1):c.334G>A (p.Gly112Ser)	LOC126859570, NRN1 (G112S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273938	NM_016588.3(NRN1):c.397T>C (p.Ser133Pro)	LOC126859570, NRN1 (S159P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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