Related gene-specific medical variations for Gene (Select 22932) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3308907	NM_012230.5(POMZP3):c.122C>T (p.Pro41Leu)	LINC03009, POMZP3 (P41L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308906	NM_012230.5(POMZP3):c.349T>C (p.Tyr117His)	LINC03009, POMZP3 (Y117H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216754	NM_012230.5(POMZP3):c.537C>A (p.Ser179Arg)	LINC03009, POMZP3 (S179R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216753	NM_012230.5(POMZP3):c.516G>T (p.Arg172Ser)	LINC03009, POMZP3 (R172S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216752	NM_012230.5(POMZP3):c.416C>G (p.Ser139Cys)	LINC03009, POMZP3 (S139C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216751	NM_012230.5(POMZP3):c.332A>T (p.Asp111Val)	LINC03009, POMZP3 (D111V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216750	NM_012230.5(POMZP3):c.245T>C (p.Leu82Pro)	LINC03009, POMZP3 (L82P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216749	NM_012230.5(POMZP3):c.203T>G (p.Leu68Arg)	LINC03009, POMZP3 (L68R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557566	NM_012230.5(POMZP3):c.158A>G (p.Glu53Gly)	LINC03009, POMZP3 (E53G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556403	NM_012230.5(POMZP3):c.467T>A (p.Ile156Asn)	LINC03009, POMZP3 (I156N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342826	NM_012230.5(POMZP3):c.22C>G (p.Leu8Val)	LINC03009, POMZP3 (L8V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2268717	NM_012230.5(POMZP3):c.540G>C (p.Gln180His)	LINC03009, POMZP3 (Q180H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance