Related gene-specific medical variations for Gene (Select 7257) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3183777	NM_005999.3(TSNAX):c.809A>G (p.His270Arg)	TSNAX, TSNAX-DISC1 (H270R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183776	NM_005999.3(TSNAX):c.665G>A (p.Arg222His)	TSNAX, TSNAX-DISC1 (R222H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606496	NM_005999.3(TSNAX):c.556G>A (p.Asp186Asn)	TSNAX, TSNAX-DISC1 (D186N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597437	NM_005999.3(TSNAX):c.712G>A (p.Glu238Lys)	TSNAX, TSNAX-DISC1 (E238K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547198	NM_005999.3(TSNAX):c.22G>C (p.Gly8Arg)	LOC126806044, TSNAX +1 more (G8R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2543141	NM_005999.3(TSNAX):c.457A>G (p.Ile153Val)	TSNAX, TSNAX-DISC1 (I153V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2478486	NM_005999.3(TSNAX):c.664C>T (p.Arg222Cys)	TSNAX, TSNAX-DISC1 (R222C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356251	NM_005999.3(TSNAX):c.751G>A (p.Ala251Thr)	TSNAX, TSNAX-DISC1 (A251T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325840	NM_005999.3(TSNAX):c.656A>T (p.Gln219Leu)	TSNAX, TSNAX-DISC1 (Q219L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791017	NM_005999.3(TSNAX):c.450A>G (p.Lys150=)	TSNAX, TSNAX-DISC1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 784454	NM_005999.3(TSNAX):c.54C>T (p.Phe18=)	LOC126806044, TSNAX +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 783966	NM_005999.3(TSNAX):c.368-8G>A	TSNAX-DISC1, TSNAX	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 718408	NM_005999.3(TSNAX):c.50A>G (p.Asn17Ser)	TSNAX-DISC1, LOC126806044 +1 more (N17S)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign