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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLCO1B3, SLCO1B3-SLCO1B7
(R23C)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(R29fs +1 more)
Deletion
(frameshift variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(S138I +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(S121del +1 more)
Deletion
(inframe_deletion)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(T291S +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(I355V +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
+1 more
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(L374S +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
+1 more
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(T386N +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(Y397C +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(E403K +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(P427A +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(P427R +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(I534T +1 more)
Single nucleotide variant
(missense variant)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(L646I +1 more)
Single nucleotide variant
(missense variant +1 more)
Rotor syndrome
GUncertain significance
SLCO1B3, SLCO1B3-SLCO1B7
(N674S +1 more)
Single nucleotide variant
(missense variant +1 more)
Rotor syndrome
+1 more
GUncertain significance
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