"Neuberg Centre For Genomic Medicine, NCGM"[submitter] AND "UGT1A9"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235021	NM_000463.3(UGT1A1):c.92T>G (p.Leu31Arg)	UGT1A, UGT1A1 +8 more (L31R)	Single nucleotide variant (missense variant +1 more)	Crigler-Najjar syndrome type 1	GUncertain significance
Select item 160236	NM_000463.3(UGT1A1):c.322C>T (p.Arg108Cys)	UGT1A, UGT1A1 +8 more (R108C)	Single nucleotide variant (missense variant +1 more)	Hyperbilirubinemia +4 more	GUncertain significance
Select item 266037	NM_000463.3(UGT1A1):c.353dup (p.Asp119fs)	UGT1A3, UGT1A6 +8 more (D119fs)	Duplication (frameshift variant +1 more)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 1339104	NM_000463.3(UGT1A1):c.358T>C (p.Ser120Pro)	UGT1A, UGT1A1 +8 more (S120P)	Single nucleotide variant (missense variant +1 more)	Crigler-Najjar syndrome, type II +1 more	GUncertain significance
Select item 2627409	NM_000463.3(UGT1A1):c.418del (p.Leu140fs)	UGT1A10, UGT1A +8 more (L140fs)	Deletion (frameshift variant +1 more)	Crigler-Najjar syndrome, type II	GLikely pathogenic
Select item 12281	NM_000463.3(UGT1A1):c.1456T>G (p.Tyr486Asp)	UGT1A, UGT1A1 +8 more (Y486D +4 more)	Single nucleotide variant (missense variant)	Crigler-Najjar syndrome, type II +7 more	GPathogenic/Likely pathogenic

ClinVar