Related gene-specific medical variations for Gene (Select 9715) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3199720	NM_003461.5(ZYX):c.230C>T (p.Pro77Leu)	FAM131B, ZYX (P77L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3199718	NM_003461.5(ZYX):c.151G>A (p.Gly51Arg)	FAM131B, ZYX (G51R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2658116	NM_003461.5(ZYX):c.192C>T (p.Pro64=)	FAM131B, ZYX	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2593165	NM_003461.5(ZYX):c.20C>T (p.Ser7Phe)	FAM131B, ZYX (S7F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260396	NM_003461.5(ZYX):c.152G>A (p.Gly51Glu)	FAM131B, ZYX (G51E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 784501	NM_003461.5(ZYX):c.188T>G (p.Ile63Ser)	FAM131B, ZYX (I63S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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