ClinVar Miner

List of variants in gene combination LURAP1L, TYRP1 reported as likely benign for not provided

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Gene type:
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Total variants: 141
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HGVS dbSNP gnomAD frequency
NM_000550.3(TYRP1):c.1082-8G>A rs79992094 0.00650
NM_000550.3(TYRP1):c.1500G>A (p.Leu500=) rs34060600 0.00644
NM_000550.3(TYRP1):c.*509C>A rs74941076 0.00443
NM_000550.3(TYRP1):c.977G>A (p.Arg326His) rs16929374 0.00383
NM_000550.3(TYRP1):c.1554G>C (p.Gln518His) rs41305647 0.00108
NM_000550.3(TYRP1):c.1029C>T (p.Asp343=) rs145061390 0.00089
NM_000550.3(TYRP1):c.1579G>C (p.Glu527Gln) rs570548703 0.00051
NM_000550.3(TYRP1):c.1514G>A (p.Arg505His) rs150899857 0.00048
NM_000550.3(TYRP1):c.914-4G>T rs376740467 0.00038
NM_000550.3(TYRP1):c.1138G>T (p.Ala380Ser) rs184910238 0.00022
NM_000550.3(TYRP1):c.1081+18G>A rs371052314 0.00006
NM_000550.3(TYRP1):c.1261+16A>G rs371479464 0.00005
NM_000550.3(TYRP1):c.1082-5T>A rs201296701 0.00003
NM_000550.3(TYRP1):c.1082-17C>T rs763824366 0.00002
NM_000550.3(TYRP1):c.1215C>A (p.Thr405=) rs1377897702 0.00002
NM_000550.3(TYRP1):c.1262-4T>C rs776208791 0.00002
NM_000550.3(TYRP1):c.1408+10G>A rs748825367 0.00002
NM_000550.3(TYRP1):c.1509C>T (p.Ala503=) rs768848671 0.00002
NM_000550.3(TYRP1):c.918C>T (p.Thr306=) rs375435167 0.00002
NM_000550.3(TYRP1):c.1002T>C (p.Ala334=) rs761970281 0.00001
NM_000550.3(TYRP1):c.1032G>A (p.Thr344=) rs766894672 0.00001
NM_000550.3(TYRP1):c.1173C>T (p.Thr391=) rs772791094 0.00001
NM_000550.3(TYRP1):c.1326A>T (p.Pro442=) rs774618643 0.00001
NM_000550.3(TYRP1):c.933T>C (p.Ile311=) rs1818182191 0.00001
NM_000550.3(TYRP1):c.1002T>A (p.Ala334=)
NM_000550.3(TYRP1):c.1035T>G (p.Pro345=)
NM_000550.3(TYRP1):c.1074A>G (p.Thr358=)
NM_000550.3(TYRP1):c.1081+10T>C
NM_000550.3(TYRP1):c.1081+11G>A
NM_000550.3(TYRP1):c.1081+13A>C
NM_000550.3(TYRP1):c.1081+19T>C
NM_000550.3(TYRP1):c.1081+19T>G
NM_000550.3(TYRP1):c.1081+7A>C
NM_000550.3(TYRP1):c.1081+8_1081+10dup
NM_000550.3(TYRP1):c.1082-10A>G
NM_000550.3(TYRP1):c.1082-12C>T rs751108729
NM_000550.3(TYRP1):c.1082-20C>T
NM_000550.3(TYRP1):c.1082-5T>C
NM_000550.3(TYRP1):c.1098G>A (p.Thr366=)
NM_000550.3(TYRP1):c.1101A>G (p.Gly367=)
NM_000550.3(TYRP1):c.1104G>A (p.Lys368=)
NM_000550.3(TYRP1):c.1120C>A (p.Arg374=)
NM_000550.3(TYRP1):c.1131C>T (p.His377=)
NM_000550.3(TYRP1):c.1135T>C (p.Leu379=)
NM_000550.3(TYRP1):c.1140T>A (p.Ala380=)
NM_000550.3(TYRP1):c.1143T>C (p.His381=)
NM_000550.3(TYRP1):c.1146A>C (p.Leu382=)
NM_000550.3(TYRP1):c.1146A>G (p.Leu382=)
NM_000550.3(TYRP1):c.1149C>T (p.Phe383=)
NM_000550.3(TYRP1):c.1155T>C (p.Asn385=)
NM_000550.3(TYRP1):c.1164G>A (p.Gly388=)
NM_000550.3(TYRP1):c.1179G>A (p.Leu393=)
NM_000550.3(TYRP1):c.1191T>C (p.Asp397=)
NM_000550.3(TYRP1):c.1197T>A (p.Ile399=)
NM_000550.3(TYRP1):c.1206C>T (p.Leu402=)
NM_000550.3(TYRP1):c.1212C>T (p.His404=)
NM_000550.3(TYRP1):c.1218C>T (p.Phe406=)
NM_000550.3(TYRP1):c.1261+14A>T
NM_000550.3(TYRP1):c.1261+15T>C
NM_000550.3(TYRP1):c.1261+16A>T
NM_000550.3(TYRP1):c.1261+17T>C rs1168799219
NM_000550.3(TYRP1):c.1261+18G>A
NM_000550.3(TYRP1):c.1261+19C>A
NM_000550.3(TYRP1):c.1261+20C>G
NM_000550.3(TYRP1):c.1261+7C>T
NM_000550.3(TYRP1):c.1261+9T>C
NM_000550.3(TYRP1):c.1262-11G>T
NM_000550.3(TYRP1):c.1262-18G>A
NM_000550.3(TYRP1):c.1262-18G>T
NM_000550.3(TYRP1):c.1262-20T>C rs2118272395
NM_000550.3(TYRP1):c.1262-6del rs772476958
NM_000550.3(TYRP1):c.1262-8T>C
NM_000550.3(TYRP1):c.1279T>C (p.Leu427=) rs148782717
NM_000550.3(TYRP1):c.1305T>C (p.Asn435=)
NM_000550.3(TYRP1):c.1314C>T (p.Tyr438=)
NM_000550.3(TYRP1):c.1323G>T (p.Val441=)
NM_000550.3(TYRP1):c.1326A>G (p.Pro442=)
NM_000550.3(TYRP1):c.1335C>A (p.Pro445=)
NM_000550.3(TYRP1):c.1341C>T (p.Val447=)
NM_000550.3(TYRP1):c.1344C>G (p.Thr448=)
NM_000550.3(TYRP1):c.1344C>T (p.Thr448=)
NM_000550.3(TYRP1):c.1392T>C (p.Tyr464=)
NM_000550.3(TYRP1):c.1401A>G (p.Gln467=)
NM_000550.3(TYRP1):c.1408+10G>C
NM_000550.3(TYRP1):c.1408+16G>C
NM_000550.3(TYRP1):c.1408+18A>G
NM_000550.3(TYRP1):c.1408+18_1408+20dup rs2118273529
NM_000550.3(TYRP1):c.1408+18_1408+21dup
NM_000550.3(TYRP1):c.1408+20T>C
NM_000550.3(TYRP1):c.1408+23dup
NM_000550.3(TYRP1):c.1408+7G>T
NM_000550.3(TYRP1):c.1408+9T>A
NM_000550.3(TYRP1):c.1409-11T>C
NM_000550.3(TYRP1):c.1409-18_1409-15dup
NM_000550.3(TYRP1):c.1409-18_1409-17insATA
NM_000550.3(TYRP1):c.1409-18_1409-17insATCA
NM_000550.3(TYRP1):c.1409-18_1409-17insATCT
NM_000550.3(TYRP1):c.1409-19T>A
NM_000550.3(TYRP1):c.1409-20T>G rs1818307190
NM_000550.3(TYRP1):c.1409-8C>A
NM_000550.3(TYRP1):c.1431G>A (p.Glu477=)
NM_000550.3(TYRP1):c.1440C>A (p.Ala480=)
NM_000550.3(TYRP1):c.1446A>G (p.Ala482=)
NM_000550.3(TYRP1):c.1455C>A (p.Gly485=)
NM_000550.3(TYRP1):c.1455C>T (p.Gly485=) rs939397722
NM_000550.3(TYRP1):c.1464A>G (p.Leu488=)
NM_000550.3(TYRP1):c.1473A>G (p.Ala491=)
NM_000550.3(TYRP1):c.1476C>G (p.Leu492=)
NM_000550.3(TYRP1):c.1491T>G (p.Ala497=)
NM_000550.3(TYRP1):c.1497T>C (p.Tyr499=)
NM_000550.3(TYRP1):c.1500G>C (p.Leu500=)
NM_000550.3(TYRP1):c.1500G>T (p.Leu500=) rs34060600
NM_000550.3(TYRP1):c.1506T>C (p.Arg502=)
NM_000550.3(TYRP1):c.1510A>C (p.Arg504=)
NM_000550.3(TYRP1):c.1542C>G (p.Leu514=)
NM_000550.3(TYRP1):c.1542C>T (p.Leu514=)
NM_000550.3(TYRP1):c.1551T>C (p.Asp517=)
NM_000550.3(TYRP1):c.1554G>A (p.Gln518=)
NM_000550.3(TYRP1):c.1560A>G (p.Gln520=) rs773136421
NM_000550.3(TYRP1):c.1566T>C (p.Tyr522=)
NM_000550.3(TYRP1):c.1572_1575dup (p.Tyr526fs)
NM_000550.3(TYRP1):c.1578T>C (p.Tyr526=)
NM_000550.3(TYRP1):c.1584del (p.Lys528fs)
NM_000550.3(TYRP1):c.1584dup (p.Leu529fs)
NM_000550.3(TYRP1):c.1596T>C (p.Pro532=)
NM_000550.3(TYRP1):c.1596T>G (p.Pro532=)
NM_000550.3(TYRP1):c.914-16C>A
NM_000550.3(TYRP1):c.914-16C>T rs768319932
NM_000550.3(TYRP1):c.914-17C>G
NM_000550.3(TYRP1):c.914-17C>T
NM_000550.3(TYRP1):c.914-5T>C
NM_000550.3(TYRP1):c.914-5_914-3del rs2118247975
NM_000550.3(TYRP1):c.914-9T>C
NM_000550.3(TYRP1):c.927G>T (p.Gly309=)
NM_000550.3(TYRP1):c.936G>A (p.Arg312=)
NM_000550.3(TYRP1):c.948T>C (p.Ala316=)
NM_000550.3(TYRP1):c.975A>G (p.Gln325=)
NM_000550.3(TYRP1):c.984T>C (p.Pro328=)
NM_000550.3(TYRP1):c.993G>A (p.Gln331=)
NM_000550.3(TYRP1):c.996T>C (p.Asp332=)
NM_000550.3(TYRP1):c.999C>T (p.Val333=)

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