"Ambry Genetics"[submitter] AND "TNIP2"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2549639	NM_024309.4(TNIP2):c.1183G>A (p.Ala395Thr)	TNIP2 (A312T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3180372	NM_024309.4(TNIP2):c.1181G>A (p.Gly394Asp)	TNIP2 (G287D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180371	NM_024309.4(TNIP2):c.1142C>T (p.Ser381Phe)	TNIP2 (S298F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482893	NM_024309.4(TNIP2):c.1045G>C (p.Ala349Pro)	TNIP2 (A349P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593550	NM_024309.4(TNIP2):c.1034G>A (p.Arg345Gln)	TNIP2 (R345Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2288351	NM_024309.4(TNIP2):c.1006C>T (p.His336Tyr)	TNIP2 (H253Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320177	NM_024309.4(TNIP2):c.994G>A (p.Ala332Thr)	TNIP2 (A225T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2350130	NM_024309.4(TNIP2):c.882G>C (p.Glu294Asp)	TNIP2 (E294D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245754	NM_024309.4(TNIP2):c.872C>T (p.Ala291Val)	TNIP2 (A291V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341485	NM_024309.4(TNIP2):c.865C>T (p.Arg289Trp)	TNIP2 (R182W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180377	NM_024309.4(TNIP2):c.717G>C (p.Arg239Ser)	TNIP2 (R132S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3180376	NM_024309.4(TNIP2):c.716G>C (p.Arg239Thr)	TNIP2 (R132T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328470	NM_024309.4(TNIP2):c.712G>T (p.Val238Leu)	TNIP2 (V238L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356824	NM_024309.4(TNIP2):c.685C>T (p.Arg229Cys)	TNIP2 (R122C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549909	NM_024309.4(TNIP2):c.684G>T (p.Gln228His)	TNIP2 (Q121H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541296	NM_024309.4(TNIP2):c.667C>T (p.Leu223Phe)	TNIP2 (L116F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602189	NM_024309.4(TNIP2):c.650T>C (p.Val217Ala)	TNIP2 (V110A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372275	NM_024309.4(TNIP2):c.632G>A (p.Arg211Gln)	TNIP2 (R104Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180375	NM_024309.4(TNIP2):c.614A>G (p.Lys205Arg)	TNIP2 (K205R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325768	NM_024309.4(TNIP2):c.550G>C (p.Glu184Gln)	TNIP2 (E77Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385959	NM_024309.4(TNIP2):c.463C>T (p.Arg155Trp)	TNIP2 (R48W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280987	NM_024309.4(TNIP2):c.441G>C (p.Leu147Phe)	TNIP2 (L40F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540639	NM_024309.4(TNIP2):c.433C>T (p.Arg145Cys)	LOC129992055, TNIP2 (R145C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312487	NM_024309.4(TNIP2):c.424G>A (p.Val142Ile)	LOC129992055, TNIP2 (V35I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2549015	NM_024309.4(TNIP2):c.421G>A (p.Asp141Asn)	LOC129992055, TNIP2 (D141N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279087	NM_024309.4(TNIP2):c.356G>A (p.Arg119Gln)	TNIP2 (R12Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276529	NM_024309.4(TNIP2):c.347A>C (p.Gln116Pro)	TNIP2 (Q116P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221459	NM_024309.4(TNIP2):c.335T>G (p.Leu112Arg)	TNIP2 (L112R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180374	NM_024309.4(TNIP2):c.224G>A (p.Arg75Gln)	LOC129992057, TNIP2 (R75Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3180373	NM_024309.4(TNIP2):c.215C>T (p.Ala72Val)	LOC129992057, TNIP2 (A72V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2609272	NM_024309.4(TNIP2):c.190G>A (p.Val64Met)	LOC129992057, TNIP2 (V64M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2551893	NM_024309.4(TNIP2):c.149C>A (p.Ala50Asp)	LOC129992057, TNIP2 (A50D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2518824	NM_024309.4(TNIP2):c.108C>G (p.Asp36Glu)	LOC129992057, TNIP2 (D36E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2467890	NM_024309.4(TNIP2):c.36G>C (p.Glu12Asp)	LOC129992057, TNIP2 (E12D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2352160	NM_024309.4(TNIP2):c.8G>A (p.Arg3Gln)	LOC129992057, TNIP2 (R3Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 35