"Ambry Genetics"[submitter] AND "PARP15"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 2262638	NM_001113523.3(PARP15):c.281T>C (p.Ile94Thr)	PARP15 (I94T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233796	NM_001113523.3(PARP15):c.353G>A (p.Gly118Glu)	PARP15 (G118E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367264	NM_001113523.3(PARP15):c.368G>A (p.Arg123Gln)	PARP15 (R123Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2335246	NM_001113523.3(PARP15):c.391C>T (p.Pro131Ser)	PARP15 (P131S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238939	NM_001113523.3(PARP15):c.400C>G (p.Gln134Glu)	PARP15 (Q134E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530518	NM_001113523.3(PARP15):c.506C>G (p.Ala169Gly)	PARP15 (A169G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2605384	NM_001113523.3(PARP15):c.559A>G (p.Ile187Val)	PARP15 (I187V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2551126	NM_001113523.3(PARP15):c.811C>T (p.Pro271Ser)	PARP15 (P271S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2328638	NM_001113523.3(PARP15):c.829C>A (p.Pro277Thr)	PARP15 (P277T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2479595	NM_001113523.3(PARP15):c.871A>C (p.Lys291Gln)	PARP15 (K291Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2402353	NM_001113523.3(PARP15):c.992G>A (p.Arg331Gln)	PARP15 (R205Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214603	NM_001113523.3(PARP15):c.1083T>G (p.Asp361Glu)	PARP15 (D235E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251498	NM_001113523.3(PARP15):c.1151T>G (p.Val384Gly)	PARP15 (V150G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2212503	NM_001113523.3(PARP15):c.1294T>C (p.Ser432Pro)	PARP15 (S198P +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2481136	NM_001113523.3(PARP15):c.1349C>T (p.Pro450Leu)	PARP15 (P450L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2221547	NM_001113523.3(PARP15):c.1544G>A (p.Arg515Gln)	PARP15 (R212Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
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 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
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 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

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Items: 26