"Ambry Genetics"[submitter] AND "UGT1A9"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330847	NM_021027.3(UGT1A9):c.28C>A (p.Leu10Ile)	UGT1A, UGT1A10 +2 more (L10I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246962	NM_021027.3(UGT1A9):c.70G>A (p.Glu24Lys)	UGT1A, UGT1A10 +2 more (E24K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186132	NM_021027.3(UGT1A9):c.101A>G (p.Asp34Gly)	UGT1A, UGT1A10 +2 more (D34G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186133	NM_021027.3(UGT1A9):c.128C>T (p.Ser43Leu)	UGT1A, UGT1A10 +2 more (S43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186134	NM_021027.3(UGT1A9):c.185T>C (p.Val62Ala)	UGT1A, UGT1A10 +2 more (V62A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556431	NM_021027.3(UGT1A9):c.217A>G (p.Thr73Ala)	UGT1A, UGT1A10 +2 more (T73A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591293	NM_021027.3(UGT1A9):c.224A>G (p.Lys75Arg)	UGT1A, UGT1A10 +2 more (K75R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790441	NM_021027.3(UGT1A9):c.225G>A (p.Lys75=)	UGT1A9, UGT1A +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3330848	NM_021027.3(UGT1A9):c.274G>C (p.Ala92Pro)	UGT1A, UGT1A10 +2 more (A92P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330843	NM_021027.3(UGT1A9):c.343G>A (p.Asp115Asn)	UGT1A, UGT1A10 +2 more (D115N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457562	NM_021027.3(UGT1A9):c.377G>A (p.Ser126Asn)	UGT1A, UGT1A10 +2 more (S126N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241585	NM_021027.3(UGT1A9):c.397T>A (p.Leu133Ile)	UGT1A, UGT1A10 +2 more (L133I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186135	NM_021027.3(UGT1A9):c.429T>G (p.Asp143Glu)	UGT1A, UGT1A10 +2 more (D143E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327957	NM_021027.3(UGT1A9):c.463T>G (p.Leu155Val)	UGT1A, UGT1A10 +2 more (L155V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604126	NM_021027.3(UGT1A9):c.512G>T (p.Gly171Val)	UGT1A, UGT1A10 +2 more (G171V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455120	NM_021027.3(UGT1A9):c.524A>G (p.His175Arg)	UGT1A, UGT1A10 +2 more (H175R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186136	NM_021027.3(UGT1A9):c.553G>A (p.Ala185Thr)	UGT1A, UGT1A10 +2 more (A185T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330846	NM_021027.3(UGT1A9):c.559C>T (p.Leu187Phe)	UGT1A, UGT1A10 +2 more (L187F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537207	NM_021027.3(UGT1A9):c.616A>G (p.Arg206Gly)	UGT1A, UGT1A10 +2 more (R206G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269188	NM_021027.3(UGT1A9):c.662A>G (p.His221Arg)	UGT1A, UGT1A10 +2 more (H221R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330845	NM_021027.3(UGT1A9):c.664C>T (p.Arg222Cys)	UGT1A, UGT1A10 +2 more (R222C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186137	NM_021027.3(UGT1A9):c.680C>T (p.Ala227Val)	UGT1A, UGT1A10 +2 more (A227V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330844	NM_021027.3(UGT1A9):c.712C>T (p.Pro238Ser)	UGT1A, UGT1A10 +2 more (P238S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186138	NM_021027.3(UGT1A9):c.764C>T (p.Thr255Met)	UGT1A, UGT1A10 +2 more (T255M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520043	NM_021027.3(UGT1A9):c.769T>G (p.Phe257Val)	UGT1A, UGT1A10 +2 more (F257V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186139	NM_021027.3(UGT1A9):c.773T>C (p.Val258Ala)	UGT1A, UGT1A10 +2 more (V258A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288007	NM_019077.3(UGT1A7):c.68C>A (p.Ala23Asp)	UGT1A, UGT1A10 +3 more (A23D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186116	NM_019077.3(UGT1A7):c.104G>A (p.Gly35Glu)	UGT1A, UGT1A10 +3 more (G35E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348238	NM_019077.3(UGT1A7):c.172G>T (p.Val58Phe)	UGT1A, UGT1A10 +3 more (V58F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186117	NM_019077.3(UGT1A7):c.274G>A (p.Val92Ile)	UGT1A, UGT1A10 +3 more (V92I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252023	NM_019077.3(UGT1A7):c.283G>A (p.Asp95Asn)	UGT1A, UGT1A10 +3 more (D95N)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2241508	NM_019077.3(UGT1A7):c.364T>C (p.Ser122Pro)	UGT1A, UGT1A10 +3 more (S122P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466343	NM_019077.3(UGT1A7):c.467T>C (p.Ile156Thr)	UGT1A, UGT1A10 +3 more (I156T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186118	NM_019077.3(UGT1A7):c.475A>G (p.Lys159Glu)	UGT1A, UGT1A10 +3 more (K159E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458203	NM_019077.3(UGT1A7):c.476A>G (p.Lys159Arg)	UGT1A, UGT1A10 +3 more (K159R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186119	NM_019077.3(UGT1A7):c.514A>G (p.Ile172Val)	UGT1A, UGT1A10 +3 more (I172V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3186120	NM_019077.3(UGT1A7):c.553G>A (p.Ala185Thr)	UGT1A, UGT1A10 +3 more (A185T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357994	NM_019077.3(UGT1A7):c.602T>A (p.Met201Lys)	UGT1A, UGT1A10 +3 more (M201K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276662	NM_019077.3(UGT1A7):c.636G>T (p.Met212Ile)	UGT1A, UGT1A10 +3 more (M212I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186121	NM_019077.3(UGT1A7):c.644A>G (p.Glu215Gly)	UGT1A, UGT1A10 +3 more (E215G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215584	NM_019077.3(UGT1A7):c.676A>G (p.Asn226Asp)	UGT1A, UGT1A10 +3 more (N226D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186122	NM_019077.3(UGT1A7):c.780G>C (p.Glu260Asp)	UGT1A, UGT1A10 +3 more (E260D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2593034	NM_019077.3(UGT1A7):c.782A>G (p.Tyr261Cys)	UGT1A, UGT1A10 +3 more (Y261C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354908	NM_019077.3(UGT1A7):c.802A>C (p.Asn268His)	UGT1A, UGT1A10 +3 more (N268H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3186123	NM_019077.3(UGT1A7):c.820G>A (p.Gly274Ser)	UGT1A, UGT1A10 +3 more (G274S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535303	NM_019077.3(UGT1A7):c.827A>G (p.Asn276Ser)	UGT1A, UGT1A10 +3 more (N276S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330837	NM_019077.3(UGT1A7):c.851C>A (p.Pro284His)	UGT1A, UGT1A10 +3 more (P284H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2690422	NM_001072.4(UGT1A6):c.16C>T (p.Arg6Cys)	UGT1A, UGT1A10 +4 more (R6C)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 3186115	NM_001072.4(UGT1A6):c.85C>A (p.Leu29Met)	UGT1A, UGT1A10 +4 more (L29M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464005	NM_001072.4(UGT1A6):c.124A>G (p.Met42Val)	UGT1A, UGT1A10 +4 more (M42V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186110	NM_001072.4(UGT1A6):c.130G>C (p.Asp44His)	UGT1A, UGT1A10 +4 more (D44H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330836	NM_001072.4(UGT1A6):c.142G>A (p.Val48Ile)	UGT1A, UGT1A10 +4 more (V48I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 811907	NM_001072.4(UGT1A6):c.146T>G (p.Leu49Arg)	UGT1A, UGT1A10 +4 more (L49R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405375	NM_001072.4(UGT1A6):c.154C>T (p.Arg52Trp)	UGT1A, UGT1A10 +4 more (R52W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480793	NM_001072.4(UGT1A6):c.206A>G (p.Glu69Gly)	UGT1A, UGT1A10 +4 more (E69G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535022	NM_001072.4(UGT1A6):c.229A>G (p.Ile77Val)	UGT1A, UGT1A10 +4 more (I77V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519846	NM_001072.4(UGT1A6):c.268C>T (p.Arg90Cys)	UGT1A, UGT1A10 +4 more (R90C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369994	NM_001072.4(UGT1A6):c.293A>G (p.His98Arg)	UGT1A, UGT1A10 +4 more (H98R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404566	NM_001072.4(UGT1A6):c.371T>A (p.Ile124Asn)	UGT1A, UGT1A10 +4 more (I124N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206502	NM_001072.4(UGT1A6):c.433G>C (p.Asp145His)	UGT1A, UGT1A10 +4 more (D145H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254557	NM_001072.4(UGT1A6):c.454G>A (p.Ala152Thr)	UGT1A, UGT1A10 +4 more (A152T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250118	NM_001072.4(UGT1A6):c.496C>T (p.Pro166Ser)	UGT1A, UGT1A10 +4 more (P166S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492344	NM_001072.4(UGT1A6):c.517G>A (p.Gly173Ser)	UGT1A, UGT1A10 +4 more (G173S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508831	NM_001072.4(UGT1A6):c.523C>G (p.Pro175Ala)	UGT1A, UGT1A10 +4 more (P175A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328917	NM_001072.4(UGT1A6):c.530C>G (p.Ser177Cys)	UGT1A, UGT1A10 +4 more (S177C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377504	NM_001072.4(UGT1A6):c.623G>A (p.Arg208Gln)	UGT1A, UGT1A10 +4 more (R208Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330835	NM_001072.4(UGT1A6):c.661C>A (p.Leu221Ile)	UGT1A, UGT1A10 +4 more (L221I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186112	NM_001072.4(UGT1A6):c.713A>G (p.Lys238Arg)	UGT1A, UGT1A10 +4 more (K238R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186113	NM_001072.4(UGT1A6):c.731T>A (p.Ile244Asn)	UGT1A, UGT1A10 +4 more (I244N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330834	NM_001072.4(UGT1A6):c.740A>G (p.Tyr247Cys)	UGT1A, UGT1A10 +4 more (Y247C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538376	NM_001072.4(UGT1A6):c.754G>T (p.Val252Phe)	UGT1A, UGT1A10 +4 more (V252F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608310	NM_001072.4(UGT1A6):c.831C>G (p.Ile277Met)	UGT1A, UGT1A10 +4 more (I277M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218190	NM_019078.2(UGT1A5):c.13C>A (p.Leu5Ile)	UGT1A, UGT1A10 +5 more (L5I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615931	NM_019078.2(UGT1A5):c.23C>T (p.Pro8Leu)	UGT1A, UGT1A10 +5 more (P8L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186108	NM_019078.2(UGT1A5):c.134G>A (p.Arg45Gln)	UGT1A, UGT1A10 +5 more (R45Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2496017	NM_019078.2(UGT1A5):c.160A>G (p.Arg54Gly)	UGT1A, UGT1A10 +5 more (R54G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518787	NM_019078.2(UGT1A5):c.380C>G (p.Ser127Cys)	UGT1A, UGT1A10 +5 more (S127C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186109	NM_019078.2(UGT1A5):c.400A>G (p.Asn134Asp)	UGT1A, UGT1A10 +5 more (N134D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374653	NM_019078.2(UGT1A5):c.496T>C (p.Ser166Pro)	UGT1A, UGT1A10 +5 more (S166P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514875	NM_019078.2(UGT1A5):c.520A>G (p.Arg174Gly)	UGT1A, UGT1A10 +5 more (R174G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529440	NM_019078.2(UGT1A5):c.720G>C (p.Gln240His)	UGT1A, UGT1A10 +5 more (Q240H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600692	NM_019078.2(UGT1A5):c.773G>A (p.Arg258Gln)	UGT1A, UGT1A10 +5 more (R258Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552288	NM_007120.3(UGT1A4):c.11G>A (p.Gly4Glu)	UGT1A, UGT1A10 +6 more (G4E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467004	NM_007120.3(UGT1A4):c.32G>A (p.Arg11Gln)	UGT1A, UGT1A10 +6 more (R11Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3186101	NM_007120.3(UGT1A4):c.44G>T (p.Gly15Val)	UGT1A, UGT1A10 +6 more (G15V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366407	NM_007120.3(UGT1A4):c.53T>A (p.Leu18His)	UGT1A, UGT1A10 +6 more (L18H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186104	NM_007120.3(UGT1A4):c.65T>C (p.Val22Ala)	UGT1A, UGT1A10 +6 more (V22A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406536	NM_007120.3(UGT1A4):c.140C>T (p.Ala47Val)	UGT1A, UGT1A10 +6 more (A47V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3186099	NM_007120.3(UGT1A4):c.157G>T (p.Ala53Ser)	UGT1A, UGT1A10 +6 more (A53S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297777	NM_007120.3(UGT1A4):c.158C>G (p.Ala53Gly)	UGT1A, UGT1A10 +6 more (A53G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186100	NM_007120.3(UGT1A4):c.167A>G (p.His56Arg)	UGT1A, UGT1A10 +6 more (H56R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2465817	NM_007120.3(UGT1A4):c.257A>G (p.Gln86Arg)	UGT1A, UGT1A10 +6 more (Q86R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459401	NM_007120.3(UGT1A4):c.274G>A (p.Val92Ile)	UGT1A, UGT1A10 +6 more (V92I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483405	NM_007120.3(UGT1A4):c.295G>C (p.Gly99Arg)	UGT1A, UGT1A10 +6 more (G99R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467792	NM_007120.3(UGT1A4):c.334A>G (p.Arg112Gly)	UGT1A, UGT1A10 +6 more (R112G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495923	NM_007120.3(UGT1A4):c.348T>G (p.Ile116Met)	UGT1A, UGT1A10 +6 more (I116M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186103	NM_007120.3(UGT1A4):c.460G>T (p.Val154Phe)	UGT1A, UGT1A10 +6 more (V154F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366207	NM_007120.3(UGT1A4):c.476C>T (p.Ala159Val)	UGT1A, UGT1A10 +6 more (A159V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309708	NM_007120.3(UGT1A4):c.685G>T (p.Ala229Ser)	UGT1A, UGT1A10 +6 more (A229S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186105	NM_007120.3(UGT1A4):c.711G>C (p.Glu237Asp)	UGT1A, UGT1A10 +6 more (E237D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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