ClinVar Miner

List of variants in gene PLOD1 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP
NC_000001.10:g.(?_11994817)_(11994932_?)dup
NC_000001.10:g.(?_12009820)_(12012802_?)del
NC_000001.10:g.(?_12020703)_(12027148_?)dup
NM_000302.4(PLOD1):c.1023C>T (p.Gly341=) rs755056846
NM_000302.4(PLOD1):c.1026C>T (p.Ser342=) rs140159343
NM_000302.4(PLOD1):c.1063C>T (p.Arg355Trp) rs775007891
NM_000302.4(PLOD1):c.1095C>T (p.Gly365=)
NM_000302.4(PLOD1):c.1097C>T (p.Ala366Val) rs377080927
NM_000302.4(PLOD1):c.109G>A (p.Glu37Lys) rs369263247
NM_000302.4(PLOD1):c.1108C>T (p.Arg370Trp)
NM_000302.4(PLOD1):c.1117C>T (p.Arg373Cys)
NM_000302.4(PLOD1):c.1145A>C (p.Asp382Ala) rs998178222
NM_000302.4(PLOD1):c.115G>A (p.Glu39Lys)
NM_000302.4(PLOD1):c.1172A>G (p.Asn391Ser) rs763409574
NM_000302.4(PLOD1):c.1180C>T (p.Arg394Trp)
NM_000302.4(PLOD1):c.1202+3G>A rs370358836
NM_000302.4(PLOD1):c.1203-3C>T rs376288573
NM_000302.4(PLOD1):c.1216C>G (p.Pro406Ala) rs760764359
NM_000302.4(PLOD1):c.1216C>T (p.Pro406Ser)
NM_000302.4(PLOD1):c.1246T>C (p.Ser416Pro)
NM_000302.4(PLOD1):c.124C>T (p.Arg42Cys) rs202003686
NM_000302.4(PLOD1):c.1255T>C (p.Trp419Arg) rs373446893
NM_000302.4(PLOD1):c.1288C>T (p.Arg430Cys)
NM_000302.4(PLOD1):c.1334T>G (p.Val445Gly)
NM_000302.4(PLOD1):c.1349A>G (p.Tyr450Cys)
NM_000302.4(PLOD1):c.137G>A (p.Arg46His) rs142710681
NM_000302.4(PLOD1):c.1387C>T (p.Arg463Trp) rs745946511
NM_000302.4(PLOD1):c.1470+5G>A rs1553136223
NM_000302.4(PLOD1):c.1482G>C (p.Met494Ile)
NM_000302.4(PLOD1):c.1511A>G (p.His504Arg) rs555034048
NM_000302.4(PLOD1):c.1543C>T (p.His515Tyr) rs746905101
NM_000302.4(PLOD1):c.1649C>T (p.Thr550Met)
NM_000302.4(PLOD1):c.1650G>A (p.Thr550=) rs201999965
NM_000302.4(PLOD1):c.1658C>T (p.Pro553Leu) rs754569828
NM_000302.4(PLOD1):c.1667A>G (p.Tyr556Cys) rs146360295
NM_000302.4(PLOD1):c.1678A>G (p.Ile560Val)
NM_000302.4(PLOD1):c.1689G>A (p.Glu563=) rs139230801
NM_000302.4(PLOD1):c.1706T>A (p.Leu569Gln) rs773547480
NM_000302.4(PLOD1):c.1763G>T (p.Arg588Leu) rs755346019
NM_000302.4(PLOD1):c.1785C>A (p.Asn595Lys)
NM_000302.4(PLOD1):c.1789C>T (p.Pro597Ser) rs141692280
NM_000302.4(PLOD1):c.1790C>T (p.Pro597Leu) rs775321665
NM_000302.4(PLOD1):c.1828C>T (p.Arg610Trp)
NM_000302.4(PLOD1):c.184G>A (p.Glu62Lys) rs146092290
NM_000302.4(PLOD1):c.1864C>T (p.Pro622Ser)
NM_000302.4(PLOD1):c.1871C>T (p.Thr624Met)
NM_000302.4(PLOD1):c.1892A>G (p.Tyr631Cys)
NM_000302.4(PLOD1):c.1937A>G (p.Lys646Arg) rs1221992885
NM_000302.4(PLOD1):c.1960A>T (p.Met654Leu) rs1085307517
NM_000302.4(PLOD1):c.2041C>T (p.Arg681Trp)
NM_000302.4(PLOD1):c.2057A>G (p.Asn686Ser) rs747393648
NM_000302.4(PLOD1):c.2068C>T (p.Arg690Ter)
NM_000302.4(PLOD1):c.2072C>T (p.Ala691Val) rs777096767
NM_000302.4(PLOD1):c.2095A>G (p.Met699Val)
NM_000302.4(PLOD1):c.2099A>G (p.His700Arg)
NM_000302.4(PLOD1):c.2162C>T (p.Ala721Val) rs149161535
NM_000302.4(PLOD1):c.2173G>A (p.Val725Ile)
NM_000302.4(PLOD1):c.232G>T (p.Val78Phe) rs1306060482
NM_000302.4(PLOD1):c.241C>G (p.Leu81Val)
NM_000302.4(PLOD1):c.265G>T (p.Ala89Ser) rs886039207
NM_000302.4(PLOD1):c.302+5G>A
NM_000302.4(PLOD1):c.303C>T (p.Ser101=) rs147980436
NM_000302.4(PLOD1):c.307G>A (p.Asp103Asn) rs774590964
NM_000302.4(PLOD1):c.314T>A (p.Leu105Gln) rs1553133902
NM_000302.4(PLOD1):c.315_317del (p.Phe106del)
NM_000302.4(PLOD1):c.376T>G (p.Phe126Val)
NM_000302.4(PLOD1):c.407G>A (p.Arg136His)
NM_000302.4(PLOD1):c.481G>A (p.Ala161Thr) rs1553134244
NM_000302.4(PLOD1):c.508G>A (p.Glu170Lys)
NM_000302.4(PLOD1):c.526A>G (p.Ser176Gly)
NM_000302.4(PLOD1):c.52G>A (p.Ala18Thr) rs373165011
NM_000302.4(PLOD1):c.534C>A (p.Ser178Arg) rs113384442
NM_000302.4(PLOD1):c.567_572del (p.Asp189_Pro190del) rs775053632
NM_000302.4(PLOD1):c.569C>T (p.Pro190Leu)
NM_000302.4(PLOD1):c.570G>A (p.Pro190=) rs776173072
NM_000302.4(PLOD1):c.579G>A (p.Arg193=) rs1553134266
NM_000302.4(PLOD1):c.608G>A (p.Arg203His) rs145482271
NM_000302.4(PLOD1):c.613C>T (p.Arg205Cys) rs199990859
NM_000302.4(PLOD1):c.674A>G (p.His225Arg)
NM_000302.4(PLOD1):c.702C>G (p.Asp234Glu)
NM_000302.4(PLOD1):c.712G>T (p.Val238Phe) rs777914756
NM_000302.4(PLOD1):c.776G>A (p.Arg259His) rs144226170
NM_000302.4(PLOD1):c.785C>T (p.Thr262Ile) rs147940796
NM_000302.4(PLOD1):c.805G>A (p.Val269Met) rs145447578
NM_000302.4(PLOD1):c.814G>A (p.Glu272Lys)
NM_000302.4(PLOD1):c.824G>A (p.Arg275His) rs184999645
NM_000302.4(PLOD1):c.839T>C (p.Ile280Thr)
NM_000302.4(PLOD1):c.842G>A (p.Gly281Glu) rs1056398577
NM_000302.4(PLOD1):c.860C>T (p.Thr287Met)
NM_000302.4(PLOD1):c.861G>A (p.Thr287=) rs747570972
NM_000302.4(PLOD1):c.871G>A (p.Gly291Ser) rs776772692
NM_000302.4(PLOD1):c.874G>A (p.Val292Met)
NM_000302.4(PLOD1):c.893C>T (p.Thr298Met) rs879902079
NM_000302.4(PLOD1):c.920G>A (p.Arg307Gln) rs960778465
NM_000302.4(PLOD1):c.929G>A (p.Arg310Gln) rs992278231
NM_000302.4(PLOD1):c.931C>T (p.Leu311Phe) rs1438781151
NM_000302.4(PLOD1):c.947A>C (p.Lys316Thr)
NM_000302.4(PLOD1):c.949C>A (p.His317Asn) rs1287367993
NM_000302.4(PLOD1):c.965T>A (p.Ile322Asn) rs1553135172
NM_000302.4(PLOD1):c.975C>T (p.His325=) rs761576315
NM_000302.4(PLOD1):c.976-6C>A rs200825919

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