ClinVar Miner

List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000463.3(UGT1A1):c.540A>G (p.Glu180=) rs148755655 0.00201
NM_000463.3(UGT1A1):c.1122T>C (p.Gly374=) rs139698110 0.00126
NM_000463.3(UGT1A1):c.326T>C (p.Val109Ala) rs144217005 0.00098
NM_000463.3(UGT1A1):c.748T>C (p.Ser250Pro) rs57307513 0.00041
NM_000463.3(UGT1A1):c.159G>A (p.Arg53=) rs149071335 0.00036
NM_000463.3(UGT1A1):c.1352C>T (p.Pro451Leu) rs114982090 0.00018
NM_000463.3(UGT1A1):c.1026A>T (p.Pro342=) rs747062491 0.00013
NM_000463.3(UGT1A1):c.1208G>A (p.Arg403His) rs140613392 0.00011
NM_000463.3(UGT1A1):c.1495G>A (p.Val499Met) rs199723856 0.00011
NM_000463.3(UGT1A1):c.1544G>T (p.Arg515Leu) rs778667717 0.00010
NM_000463.3(UGT1A1):c.1324C>T (p.Arg442Cys) rs143033456 0.00009
NM_000463.3(UGT1A1):c.189C>T (p.Asp63=) rs191471887 0.00009
NM_000463.3(UGT1A1):c.1348C>T (p.Arg450Cys) rs201427749 0.00008
NM_000463.3(UGT1A1):c.1085G>T (p.Gly362Val) rs752968297 0.00006
NM_000463.3(UGT1A1):c.1100G>T (p.Arg367Leu) rs374047963 0.00006
NM_000463.3(UGT1A1):c.1156G>A (p.Val386Ile) rs143573365 0.00006
NM_000463.3(UGT1A1):c.1231G>T (p.Val411Leu) rs36076514 0.00006
NM_000463.3(UGT1A1):c.1470C>T (p.Asp490=) rs114123636 0.00006
NM_000463.3(UGT1A1):c.577G>A (p.Val193Met) rs375974892 0.00006
NM_000463.3(UGT1A1):c.1349G>A (p.Arg450His) rs200370335 0.00005
NM_000463.3(UGT1A1):c.142C>G (p.Gln48Glu) rs747942373 0.00005
NM_000463.3(UGT1A1):c.1458C>T (p.Tyr486=) rs142077822 0.00005
NM_000463.3(UGT1A1):c.1459C>T (p.His487Tyr) rs371183955 0.00005
NM_000463.3(UGT1A1):c.477C>T (p.Ile159=) rs199766420 0.00005
NM_000463.3(UGT1A1):c.1558A>G (p.Lys520Glu) rs553499095 0.00004
NM_000463.3(UGT1A1):c.801C>T (p.Pro267=) rs200102302 0.00004
NM_000463.3(UGT1A1):c.1099C>T (p.Arg367Cys) rs55750087 0.00003
NM_000463.3(UGT1A1):c.1207C>T (p.Arg403Cys) rs778766461 0.00003
NM_000463.3(UGT1A1):c.167A>C (p.Glu56Ala) rs140365717 0.00003
NM_000463.3(UGT1A1):c.19G>A (p.Gly7Ser) rs1006073064 0.00003
NM_000463.3(UGT1A1):c.835A>T (p.Asn279Tyr) rs397978903 0.00003
NM_000463.3(UGT1A1):c.-4C>T rs752018052 0.00002
NM_000463.3(UGT1A1):c.1175C>T (p.Pro392Leu) rs886043066 0.00002
NM_000463.3(UGT1A1):c.195G>A (p.Ser65=) rs767800703 0.00002
NM_000463.3(UGT1A1):c.817G>T (p.Val273Phe) rs143072292 0.00002
NM_000463.3(UGT1A1):c.1161C>T (p.Pro387=) rs763217521 0.00001
NM_000463.3(UGT1A1):c.1170G>A (p.Met390Ile) rs1559415443 0.00001
NM_000463.3(UGT1A1):c.137C>T (p.Ala46Val) rs886044683 0.00001
NM_000463.3(UGT1A1):c.1564G>A (p.Gly522Arg) rs746578451 0.00001
NM_000463.3(UGT1A1):c.22G>A (p.Gly8Arg) rs749552053 0.00001
NM_000463.3(UGT1A1):c.300T>C (p.Phe100=) rs374655757 0.00001
NM_000463.3(UGT1A1):c.838T>G (p.Cys280Gly) rs754213125 0.00001
NM_000463.3(UGT1A1):c.1001T>A (p.Leu334Gln) rs757687307
NM_000463.3(UGT1A1):c.1060T>A (p.Trp354Arg) rs1559414817
NM_000463.3(UGT1A1):c.1073A>C (p.Asn358Thr) rs886044684
NM_000463.3(UGT1A1):c.1084G>A (p.Gly362Ser) rs755218546
NM_000463.3(UGT1A1):c.1108A>G (p.Ile370Val) rs748989741
NM_000463.3(UGT1A1):c.1110_1150delinsGC (p.Ile370_Asn384delinsMetHis) rs1559415286
NM_000463.3(UGT1A1):c.1174C>T (p.Pro392Ser) rs1286993592
NM_000463.3(UGT1A1):c.1198A>C (p.Asn400His) rs28934877
NM_000463.3(UGT1A1):c.1322T>C (p.Met441Thr) rs202172337
NM_000463.3(UGT1A1):c.138C>T (p.Ala46=) rs886044249
NM_000463.3(UGT1A1):c.1455G>A (p.Gln485=) rs1173929998
NM_000463.3(UGT1A1):c.1555G>A (p.Gly519Arg) rs1553624227
NM_000463.3(UGT1A1):c.210C>G (p.Asp70Glu) rs1553620689
NM_000463.3(UGT1A1):c.386A>G (p.His129Arg) rs1191873899
NM_000463.3(UGT1A1):c.399C>G (p.Asn133Lys) rs1553620770
NM_000463.3(UGT1A1):c.428G>A (p.Ser143Asn) rs1559407347
NM_000463.3(UGT1A1):c.575A>G (p.Tyr192Cys) rs201093245
NM_000463.3(UGT1A1):c.907G>A (p.Val303Met) rs770930440

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