Related gene-specific medical variations for Gene (Select 79155) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327568	NM_024309.4(TNIP2):c.83G>C (p.Gly28Ala)	LOC129992057, TNIP2 (G28A)	Single nucleotide variant (5 prime UTR variant +1 more)	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 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 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 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
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