Related gene-specific medical variations for Gene (Select 93653) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3170706	NM_001369598.1(ST7):c.145A>C (p.Ser49Arg)	ST7, ST7-AS1 (S49R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3170705	NM_001369598.1(ST7):c.128A>C (p.Lys43Thr)	ST7, ST7-AS1 (K43T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2493749	NM_001369598.1(ST7):c.46A>C (p.Ile16Leu)	ST7, ST7-AS1 (I16L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2352248	NM_001369598.1(ST7):c.11C>T (p.Ala4Val)	ST7, ST7-AS1 (A4V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2333048	NM_001369598.1(ST7):c.97T>C (p.Phe33Leu)	ST7, ST7-AS1 (F33L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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