ClinVar Miner

List of variants in gene DCLRE1C reported by Baylor Genetics

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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_001033855.3(DCLRE1C):c.241C>T (p.Arg81Ter) rs121908156 0.00004
NM_001033855.3(DCLRE1C):c.109+1G>T rs143144732 0.00003
NM_001033855.3(DCLRE1C):c.1784dup (p.Ile596fs) rs1190921257 0.00003
NM_001033855.3(DCLRE1C):c.103C>G (p.His35Asp) rs121908159 0.00001
NM_001033855.3(DCLRE1C):c.1777C>T (p.Gln593Ter) rs1250826419 0.00001
NM_001033855.3(DCLRE1C):c.464+1G>A rs1162344514 0.00001
NM_001033855.3(DCLRE1C):c.465-2A>C rs1839625956 0.00001
NM_001033855.3(DCLRE1C):c.47T>C (p.Ile16Thr) rs1317003987 0.00001
NM_001033855.3(DCLRE1C):c.1103del (p.Lys368fs) rs2491775008
NM_001033855.3(DCLRE1C):c.1106dup (p.Tyr369Ter) rs2491774838
NM_001033855.3(DCLRE1C):c.1156+1G>A rs2491772724
NM_001033855.3(DCLRE1C):c.1159_1184dup (p.Asp395fs) rs2491637403
NM_001033855.3(DCLRE1C):c.1176_1179del (p.Phe393fs) rs2491637540
NM_001033855.3(DCLRE1C):c.1238del (p.Pro413fs) rs2491636150
NM_001033855.3(DCLRE1C):c.1265C>A (p.Ser422Ter) rs1354336544
NM_001033855.3(DCLRE1C):c.1319_1320del (p.Cys440fs) rs2491634111
NM_001033855.3(DCLRE1C):c.1324C>T (p.Gln442Ter) rs2491633975
NM_001033855.3(DCLRE1C):c.1350_1356del (p.Asp451fs) rs786200884
NM_001033855.3(DCLRE1C):c.1442del (p.Lys481fs) rs2131776743
NM_001033855.3(DCLRE1C):c.1442dup (p.Ala482fs) rs2131776743
NM_001033855.3(DCLRE1C):c.1492dup (p.Glu498fs) rs1588893751
NM_001033855.3(DCLRE1C):c.1513G>T (p.Glu505Ter) rs2491629802
NM_001033855.3(DCLRE1C):c.1539_1540del (p.Gly515fs) rs2491629087
NM_001033855.3(DCLRE1C):c.1574_1575del (p.Asp524_Ser525insTer) rs2491628054
NM_001033855.3(DCLRE1C):c.1628_1632del (p.Ile543fs) rs767758218
NM_001033855.3(DCLRE1C):c.1696_1699dup (p.Ser567fs) rs762761194
NM_001033855.3(DCLRE1C):c.1706dup (p.Asp569fs) rs752450605
NM_001033855.3(DCLRE1C):c.1749dup (p.Glu584fs) rs765144892
NM_001033855.3(DCLRE1C):c.1774G>T (p.Glu592Ter) rs2491621783
NM_001033855.3(DCLRE1C):c.1789del (p.Cys597fs) rs759377639
NM_001033855.3(DCLRE1C):c.1797_1818dup (p.Ser607delinsGlyTyrLeuLeuTer) rs2491620281
NM_001033855.3(DCLRE1C):c.1803_1804dup (p.Tyr602fs) rs1834728173
NM_001033855.3(DCLRE1C):c.1808_1809del (p.Tyr602_Ser603insTer) rs2491620581
NM_001033855.3(DCLRE1C):c.1830del (p.Asp611fs) rs2491620028
NM_001033855.3(DCLRE1C):c.184_191del (p.Ser62fs) rs1460843145
NM_001033855.3(DCLRE1C):c.1978_1981dup (p.Leu661Ter) rs1330020307
NM_001033855.3(DCLRE1C):c.246+2T>G rs2492298473
NM_001033855.3(DCLRE1C):c.274dup (p.Gln92fs) rs2492174062
NM_001033855.3(DCLRE1C):c.306+1G>A rs2492173028
NM_001033855.3(DCLRE1C):c.306+2T>A rs2131026813
NM_001033855.3(DCLRE1C):c.310_313del rs2130974126
NM_001033855.3(DCLRE1C):c.330_331del (p.Leu111fs) rs2492077470
NM_001033855.3(DCLRE1C):c.352G>T (p.Gly118Ter) rs1839957089
NM_001033855.3(DCLRE1C):c.362+1G>T rs1564446526
NM_001033855.3(DCLRE1C):c.416T>A (p.Leu139Ter) rs2492040094
NM_001033855.3(DCLRE1C):c.461del (p.Gly154fs) rs1404214090
NM_001033855.3(DCLRE1C):c.464+2T>C rs2492038028
NM_001033855.3(DCLRE1C):c.488_491del (p.Tyr163fs) rs2492029077
NM_001033855.3(DCLRE1C):c.538-1G>A rs2492025655
NM_001033855.3(DCLRE1C):c.571C>T (p.Arg191Ter) rs752655158
NM_001033855.3(DCLRE1C):c.595_596dup (p.His200fs) rs2492024816
NM_001033855.3(DCLRE1C):c.597C>A (p.Tyr199Ter) rs121908157
NM_001033855.3(DCLRE1C):c.671del (p.Gly224fs) rs1407251815
NM_001033855.3(DCLRE1C):c.676C>T (p.Gln226Ter) rs1564438804
NM_001033855.3(DCLRE1C):c.678+1G>A rs2492023846
NM_001033855.3(DCLRE1C):c.678+2T>G rs1215422400
NM_001033855.3(DCLRE1C):c.716del (p.Pro239fs) rs2492005406
NM_001033855.3(DCLRE1C):c.754C>T (p.Gln252Ter) rs1589050343
NM_001033855.3(DCLRE1C):c.816T>A (p.Cys272Ter) rs1346260747
NM_001033855.3(DCLRE1C):c.879G>A (p.Trp293Ter) rs2491946964
NM_001033855.3(DCLRE1C):c.928_929dup (p.Ser310fs) rs1564414831
NM_001033855.3(DCLRE1C):c.95C>T (p.Ser32Phe) rs969498121
NM_001033855.3(DCLRE1C):c.973-1G>A rs2491846909

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