Related gene-specific medical variations for Gene (Select 2907) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282819	NM_001009184.2(GRINA):c.331C>G (p.Pro111Ala)	GRINA, PARP10 (P111A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282818	NM_001009184.2(GRINA):c.152C>T (p.Pro51Leu)	GRINA, PARP10 (P51L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282817	NM_001009184.2(GRINA):c.284C>G (p.Pro95Arg)	GRINA, PARP10 (P95R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282816	NM_001009184.2(GRINA):c.625A>T (p.Ile209Phe)	GRINA, PARP10 (I209F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102560	NM_001009184.2(GRINA):c.58G>A (p.Gly20Arg)	GRINA, PARP10 (G20R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102559	NM_001009184.2(GRINA):c.409G>T (p.Gly137Cys)	GRINA, PARP10 (G137C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102558	NM_001009184.2(GRINA):c.323C>T (p.Pro108Leu)	GRINA, PARP10 (P108L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389928	NM_001009184.2(GRINA):c.67G>T (p.Gly23Trp)	GRINA, PARP10 (G23W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353219	NM_001009184.2(GRINA):c.360C>G (p.Phe120Leu)	GRINA, PARP10 (F120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335347	NM_001009184.2(GRINA):c.215G>A (p.Gly72Asp)	GRINA, PARP10 (G72D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313889	NM_001009184.2(GRINA):c.338C>T (p.Pro113Leu)	GRINA, PARP10 (P113L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311758	NM_001009184.2(GRINA):c.478G>A (p.Ala160Thr)	GRINA, PARP10 (A160T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297521	NM_001009184.2(GRINA):c.370G>C (p.Asp124His)	GRINA, PARP10 (D124H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283176	NM_001009184.2(GRINA):c.778A>G (p.Ile260Val)	GRINA, PARP10 (I260V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219126	NM_001009184.2(GRINA):c.8A>G (p.His3Arg)	GRINA, LOC124188248 +1 more (H3R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance