UGT1A10[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59158	GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	LOC129935343, LOC129935344 +1703 more	Copy number gain	See cases	GPathogenic
Select item 154206	GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	AAMP, ABCA12 +1687 more	Copy number gain	See cases	GPathogenic
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 57419	GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3	LOC129935713, LOC129935714 +1299 more	Copy number gain	See cases	GPathogenic
Select item 146683	GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3	AAMP, ABCA12 +1148 more	Copy number gain	See cases	GPathogenic
Select item 155149	GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3	LOC110120629, LOC110120691 +986 more	Copy number gain	See cases	GPathogenic
Select item 58847	GRCh38/hg38 2q36.3-37.3(chr2:226978129-236886599)x1	ACKR3, AGAP1 +393 more	Copy number loss	See cases	GPathogenic
Select item 58848	GRCh38/hg38 2q36.3-37.2(chr2:227343278-235339168)x1	CCL20, CHRND +347 more	Copy number loss	See cases	GPathogenic
Select item 59173	GRCh38/hg38 2q36.3-37.3(chr2:227803148-242086301)x3	LOC129935966, LOC129935967 +630 more	Copy number gain	See cases	GPathogenic
Select item 147843	GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3	LOC126806558, LOC126806559 +309 more	Copy number gain	See cases	GPathogenic
Select item 144756	GRCh38/hg38 2q36.3-37.3(chr2:228723579-241404867)x3	LOC132088828, LOC132088829 +576 more	Copy number gain	See cases	GPathogenic
Select item 161051	GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1	LOC129935965, LOC129935966 +455 more	Copy number loss	See cases	GPathogenic
Select item 34724	GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1	ACKR3, AGAP1 +455 more	Copy number loss	See cases	GPathogenic
Select item 58851	GRCh38/hg38 2q37.1-37.3(chr2:233420162-242086301)x1	ACKR3, AGAP1 +361 more	Copy number loss	See cases	GPathogenic
Select item 57177	GRCh38/hg38 2q37.1(chr2:233420162-233761780)x3	DGKD, DNAJB3 +16 more	Copy number gain	See cases	GUncertain significance
Select item 58852	GRCh38/hg38 2q37.1-37.3(chr2:233453611-242099155)x1	RAB17-DT, RAMP1 +359 more	Copy number loss	See cases	GPathogenic
Select item 2205121	NM_019075.4(UGT1A10):c.28G>A (p.Val10Ile)	UGT1A, UGT1A10 +1 more (V10I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257028	NM_019075.4(UGT1A10):c.31C>G (p.Pro11Ala)	UGT1A, UGT1A10 +1 more (P11A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248099	NM_019075.4(UGT1A10):c.53T>C (p.Leu18Pro)	UGT1A, UGT1A10 +1 more (L18P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522678	NM_019075.4(UGT1A10):c.62G>C (p.Gly21Ala)	UGT1A, UGT1A10 +1 more (G21A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526400	NM_019075.4(UGT1A10):c.77G>A (p.Gly26Glu)	UGT1A, UGT1A10 +1 more (G26E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186093	NM_019075.4(UGT1A10):c.158A>T (p.His53Leu)	UGT1A, UGT1A10 +1 more (H53L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330830	NM_019075.4(UGT1A10):c.272T>C (p.Met91Thr)	UGT1A, UGT1A10 +1 more (M91T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186094	NM_019075.4(UGT1A10):c.350T>C (p.Leu117Pro)	UGT1A, UGT1A10 +1 more (L117P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486578	NM_019075.4(UGT1A10):c.370T>C (p.Cys124Arg)	UGT1A, UGT1A10 +1 more (C124R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282869	NM_019075.4(UGT1A10):c.586G>C (p.Gly196Arg)	UGT1A, UGT1A10 +1 more (G196R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 775833	NM_019075.4(UGT1A10):c.597T>C (p.Asp199=)	UGT1A, UGT1A10 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2262154	NM_019075.4(UGT1A10):c.634G>C (p.Val212Leu)	UGT1A, UGT1A10 +1 more (V212L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330829	NM_019075.4(UGT1A10):c.648C>A (p.Asp216Glu)	UGT1A, UGT1A10 +1 more (D216E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2307228	NM_019075.4(UGT1A10):c.649C>A (p.His217Asn)	UGT1A, UGT1A10 +1 more (H217N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290627	NM_019075.4(UGT1A10):c.691G>A (p.Ala231Thr)	UGT1A, UGT1A10 +1 more (A231T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186095	NM_019075.4(UGT1A10):c.713C>T (p.Pro238Leu)	UGT1A, UGT1A10 +1 more (P238L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259850	NM_019075.4(UGT1A10):c.782A>G (p.Tyr261Cys)	UGT1A, UGT1A10 +1 more (Y261C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186096	NM_019075.4(UGT1A10):c.793G>A (p.Val265Met)	UGT1A, UGT1A10 +1 more (V265M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186097	NM_019075.4(UGT1A10):c.829T>C (p.Cys277Arg)	UGT1A, UGT1A10 +1 more (C277R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1263192	NM_019076.5(UGT1A8):c.855+51220C>T	UGT1A, UGT1A10 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3358191	NM_021027.3(UGT1A9):c.8G>A (p.Cys3Tyr)	UGT1A, UGT1A10 +2 more (C3Y)	Single nucleotide variant (missense variant +1 more)	UGT1A9-related disorder	GLikely benign
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 2652019	NM_021027.3(UGT1A9):c.98T>C (p.Met33Thr)	UGT1A, UGT1A10 +2 more (M33T)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
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 3055972	NM_021027.3(UGT1A9):c.196C>T (p.Leu66=)	UGT1A, UGT1A10 +2 more	Single nucleotide variant (synonymous variant +1 more)	UGT1A9-related disorder	GBenign
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 3032294	NM_021027.3(UGT1A9):c.417G>A (p.Glu139=)	UGT1A, UGT1A10 +2 more	Single nucleotide variant (synonymous variant +1 more)	UGT1A9-related disorder	GLikely benign
Select item 3041957	NM_021027.3(UGT1A9):c.423T>G (p.Ser141=)	UGT1A, UGT1A10 +2 more	Single nucleotide variant (synonymous variant +1 more)	UGT1A9-related disorder	GLikely benign
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 3038913	NM_021027.3(UGT1A9):c.432A>G (p.Ala144=)	UGT1A, UGT1A10 +2 more	Single nucleotide variant (synonymous variant +1 more)	UGT1A9-related disorder	GLikely benign
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 3046264	NM_021027.3(UGT1A9):c.500T>C (p.Val167Ala)	UGT1A, UGT1A10 +2 more (V167A)	Single nucleotide variant (missense variant +1 more)	UGT1A9-related disorder	GLikely benign
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 1289436	NM_019076.5(UGT1A8):c.855+63270T>G	UGT1A, UGT1A10 +2 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 440384	NM_019076.5(UGT1A8):c.855+63319T>G	UGT1A, UGT1A10 +2 more	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 440385	NM_019076.5(UGT1A8):c.855+63408C>A	UGT1A, UGT1A10 +3 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
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 811843	NM_019075.4(UGT1A10):c.855+44683G>A	UGT1A, UGT1A10 +3 more (M41I)	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 2690427	NM_019077.3(UGT1A7):c.192G>A (p.Trp64Ter)	UGT1A, UGT1A10 +3 more (W64*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2690429	NM_019077.3(UGT1A7):c.243C>A (p.Tyr81Ter)	UGT1A, UGT1A10 +3 more (Y81*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 993651	NM_019075.4(UGT1A10):c.855+44822C>T	UGT1A8, UGT1A9 +3 more (R88W)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 811972	NM_019075.4(UGT1A10):c.855+44828T>C	UGT1A, UGT1A10 +3 more (F90L)	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 2920843	NM_019076.5(UGT1A8):c.855+63716A>G	UGT1A, UGT1A10 +3 more (N114S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1679510	NM_019076.5(UGT1A8):c.855+63718G>A	UGT1A, UGT1A10 +3 more (G115S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 618470	NM_019077.3(UGT1A7):c.352G>T (p.Asp118Tyr)	UGT1A, UGT1A10 +3 more (D118Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
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 1330751	NM_019076.5(UGT1A8):c.855+63761_855+63762delinsGG	UGT1A, UGT1A10 +3 more (N129R)	Indel (missense variant +1 more)	not provided	GLikely benign
Select item 1330729	NM_019076.5(UGT1A8):c.855+63761A>G	UGT1A, UGT1A10 +3 more (N129S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 440386	NM_019076.5(UGT1A8):c.855+63762T>G	UGT1A8, UGT1A9 +3 more (N129K)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1333166	NM_019076.5(UGT1A8):c.855+63766_855+63767delinsAA	UGT1A7, UGT1A +3 more (R131K)	Indel (missense variant +1 more)	not provided	GBenign
Select item 440387	NM_019076.5(UGT1A8):c.855+63766C>A	UGT1A, UGT1A10 +3 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 440388	NM_019076.5(UGT1A8):c.855+63767G>A	UGT1A10, UGT1A7 +3 more (R131Q)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1330505	NM_019076.5(UGT1A8):c.855+63792G>C	UGT1A8, UGT1A9 +3 more (E139D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1330921	NM_019075.4(UGT1A10):c.855+44982G>C	UGT1A, UGT1A10 +3 more (C141S)	Single nucleotide variant (missense variant +1 more)	not provided	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 2690426	NM_019077.3(UGT1A7):c.503del (p.Phe168fs)	UGT1A, UGT1A10 +3 more (F168fs)	Deletion (frameshift variant +1 more)	not provided	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

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