Related gene-specific medical variations for Gene (Select 101927249) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3305684	NM_015009.3(PDZRN3):c.377T>G (p.Val126Gly)	PDZRN3, PDZRN3-AS1 (V126G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305682	NM_015009.3(PDZRN3):c.343G>A (p.Ala115Thr)	PDZRN3, PDZRN3-AS1 (A115T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305676	NM_015009.3(PDZRN3):c.286C>G (p.Gln96Glu)	PDZRN3, PDZRN3-AS1 (Q96E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305675	NM_015009.3(PDZRN3):c.352G>T (p.Gly118Cys)	PDZRN3, PDZRN3-AS1 (G118C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211228	NM_015009.3(PDZRN3):c.7T>G (p.Phe3Val)	PDZRN3, PDZRN3-AS1 (F3V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211227	NM_015009.3(PDZRN3):c.713C>G (p.Pro238Arg)	PDZRN3, PDZRN3-AS1 (P238R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211226	NM_015009.3(PDZRN3):c.700G>C (p.Val234Leu)	PDZRN3, PDZRN3-AS1 (V234L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211225	NM_015009.3(PDZRN3):c.65A>G (p.His22Arg)	PDZRN3, PDZRN3-AS1 (H22R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211224	NM_015009.3(PDZRN3):c.618G>C (p.Gln206His)	PDZRN3, PDZRN3-AS1 (Q206H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211223	NM_015009.3(PDZRN3):c.544A>G (p.Lys182Glu)	PDZRN3, PDZRN3-AS1 (K182E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211222	NM_015009.3(PDZRN3):c.392G>A (p.Arg131His)	PDZRN3, PDZRN3-AS1 (R131H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211218	NM_015009.3(PDZRN3):c.25G>A (p.Asp9Asn)	PDZRN3, PDZRN3-AS1 (D9N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598470	NM_015009.3(PDZRN3):c.446C>T (p.Pro149Leu)	PDZRN3, PDZRN3-AS1 (P149L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475580	NM_015009.3(PDZRN3):c.407C>G (p.Ala136Gly)	PDZRN3, PDZRN3-AS1 (A136G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471528	NM_015009.3(PDZRN3):c.686C>G (p.Ser229Trp)	PDZRN3, PDZRN3-AS1 (S229W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341603	NM_015009.3(PDZRN3):c.433G>A (p.Gly145Ser)	PDZRN3, PDZRN3-AS1 (G145S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306755	NM_015009.3(PDZRN3):c.398C>T (p.Ala133Val)	PDZRN3, PDZRN3-AS1 (A133V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299628	NM_015009.3(PDZRN3):c.31G>T (p.Asp11Tyr)	PDZRN3, PDZRN3-AS1 (D11Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248839	NM_015009.3(PDZRN3):c.182C>T (p.Ser61Leu)	PDZRN3, PDZRN3-AS1 (S61L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance