"Ambry Genetics"[submitter] AND "TYW3"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2612997	NM_138467.3(TYW3):c.49A>C (p.Lys17Gln)	TYW3 (K17Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185303	NM_138467.3(TYW3):c.193G>T (p.Val65Phe)	TYW3 (V65F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386005	NM_138467.3(TYW3):c.256A>G (p.Ile86Val)	TYW3 (I86V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2523691	NM_138467.3(TYW3):c.285T>A (p.Asp95Glu)	TYW3 (D95E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3185304	NM_138467.3(TYW3):c.290C>G (p.Thr97Ser)	TYW3 (T97S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3330454	NM_138467.3(TYW3):c.304C>T (p.Pro102Ser)	TYW3 (P102S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2214046	NM_138467.3(TYW3):c.463A>G (p.Ser155Gly)	TYW3 (S122G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185305	NM_138467.3(TYW3):c.484G>A (p.Val162Met)	TYW3 (V129M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540993	NM_138467.3(TYW3):c.499A>G (p.Ile167Val)	TYW3 (I167V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403747	NM_138467.3(TYW3):c.592A>G (p.Arg198Gly)	TYW3 (R165G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330455	NM_138467.3(TYW3):c.599C>T (p.Thr200Met)	TYW3 (T167M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509646	NM_138467.3(TYW3):c.604A>T (p.Thr202Ser)	TYW3 (T169S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185306	NM_138467.3(TYW3):c.607A>G (p.Asn203Asp)	TYW3 (N170D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568750	NM_138467.3(TYW3):c.674A>G (p.Glu225Gly)	TYW3 (E225G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185307	NM_138467.3(TYW3):c.682C>T (p.Arg228Cys)	TYW3 (R195C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance