Related gene-specific medical variations for Gene (Select 128864) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2392363	NM_080825.4(C20orf144):c.358C>G (p.Arg120Gly)	C20orf144, NECAB3 (R120G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258224	NM_080825.4(C20orf144):c.439C>G (p.Arg147Gly)	C20orf144, NECAB3 (R147G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241747	NM_080825.4(C20orf144):c.91T>C (p.Ser31Pro)	C20orf144, NECAB3 (S31P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2230034	NM_080825.4(C20orf144):c.352T>G (p.Trp118Gly)	C20orf144, NECAB3 (W118G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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