"Ambry Genetics"[submitter] AND "SLCO3A1"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351286	NM_013272.4(SLCO3A1):c.464C>T (p.Ser155Leu)	SLCO3A1 (S155L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307436	NM_013272.4(SLCO3A1):c.472G>T (p.Asp158Tyr)	SLCO3A1 (D158Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220847	NM_013272.4(SLCO3A1):c.487C>A (p.Pro163Thr)	SLCO3A1 (P163T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336237	NM_013272.4(SLCO3A1):c.518C>T (p.Thr173Ile)	SLCO3A1 (T173I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318358	NM_013272.4(SLCO3A1):c.843G>C (p.Leu281Phe)	SLCO3A1 (L281F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3320381	NM_013272.4(SLCO3A1):c.860A>G (p.Gln287Arg)	SLCO3A1 (Q287R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463164	NM_013272.4(SLCO3A1):c.886G>A (p.Ala296Thr)	SLCO3A1 (A296T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165847	NM_013272.4(SLCO3A1):c.963C>A (p.His321Gln)	SLCO3A1 (H321Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165839	NM_013272.4(SLCO3A1):c.1055C>T (p.Thr352Ile)	LOC125146356, SLCO3A1 (T352I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165840	NM_013272.4(SLCO3A1):c.1222C>T (p.Leu408Phe)	SLCO3A1 (L408F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165841	NM_013272.4(SLCO3A1):c.1361C>A (p.Pro454His)	SLCO3A1 (P454H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165842	NM_013272.4(SLCO3A1):c.1486G>C (p.Ala496Pro)	SLCO3A1 (A496P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611185	NM_013272.4(SLCO3A1):c.1520C>T (p.Thr507Met)	SLCO3A1 (T507M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341912	NM_013272.4(SLCO3A1):c.1554G>C (p.Glu518Asp)	SLCO3A1 (E518D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165843	NM_013272.4(SLCO3A1):c.1564G>A (p.Val522Met)	SLCO3A1 (V522M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3165844	NM_013272.4(SLCO3A1):c.1721T>G (p.Leu574Trp)	SLCO3A1 (L574W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479499	NM_013272.4(SLCO3A1):c.1766C>T (p.Pro589Leu)	SLCO3A1 (P589L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221293	NM_013272.4(SLCO3A1):c.1831C>A (p.Gln611Lys)	SLCO3A1 (Q611K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221294	NM_013272.4(SLCO3A1):c.1832A>G (p.Gln611Arg)	SLCO3A1 (Q611R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165845	NM_013272.4(SLCO3A1):c.1861G>A (p.Val621Ile)	SLCO3A1 (V621I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322370	NM_013272.4(SLCO3A1):c.1895C>T (p.Ala632Val)	SLCO3A1 (A632V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319274	NM_013272.4(SLCO3A1):c.1912T>G (p.Phe638Val)	SLCO3A1 (F638V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320379	NM_013272.4(SLCO3A1):c.1960C>G (p.Arg654Gly)	SLCO3A1 (R654G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165846	NM_013272.4(SLCO3A1):c.1960C>T (p.Arg654Cys)	SLCO3A1 (R654C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410865	NM_013272.4(SLCO3A1):c.1977C>G (p.His659Gln)	SLCO3A1 (H659Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247034	NM_001145044.1(SLCO3A1):c.2074A>T (p.Ser692Cys)	SLCO3A1 (S692C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26