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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2261580	NM_004622.3(TSN):c.50A>G (p.Glu17Gly)	TSN (E17G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617320	NM_004622.3(TSN):c.67G>A (p.Glu23Lys)	TSN (E23K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259655	NM_004622.3(TSN):c.197G>T (p.Gly66Val)	TSN (G66V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273341	NM_004622.3(TSN):c.550C>T (p.Leu184Phe)	TSN (L184F)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2293623	NM_004622.3(TSN):c.632A>G (p.Asp211Gly)	TSN (D211G)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

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