Related gene-specific medical variations for Gene (Select 165631) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2514057	NM_001113523.3(PARP15):c.1754C>G (p.Ser585Cys)	PARP15, LOC126806789 (S282C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2487816	NM_001113523.3(PARP15):c.41C>G (p.Pro14Arg)	LOC129937381, PARP15 (P14R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378116	NM_001113523.3(PARP15):c.59G>C (p.Arg20Thr)	LOC129937381, PARP15 (R20T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378115	NM_001113523.3(PARP15):c.101G>C (p.Gly34Ala)	LOC129937381, PARP15 (G34A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363943	NM_001113523.3(PARP15):c.1979T>C (p.Phe660Ser)	LOC126806789, PARP15 (F660S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2341134	NM_001113523.3(PARP15):c.106G>C (p.Asp36His)	LOC129937381, PARP15 (D36H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326025	NM_001113523.3(PARP15):c.1814C>T (p.Ser605Phe)	LOC126806789, PARP15 (S371F +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251071	NM_001113523.3(PARP15):c.97G>A (p.Ala33Thr)	LOC129937381, PARP15 (A33T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248215	NM_001113523.3(PARP15):c.158C>T (p.Ala53Val)	LOC129937381, PARP15 (A53V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2229079	NM_001113523.3(PARP15):c.1778C>T (p.Ala593Val)	LOC126806789, PARP15 (A593V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance