| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.67940068G>A | CA396375566 | LCAT | c.1159C>T (p.Gln387Ter) c.162C>T c.897C>T (n.897C>T) | |
| 16 | g.67940068G>C | CA396375567 | LCAT | c.1159C>G (p.Gln387Glu) c.162C>G c.897C>G (n.897C>G) | |
| 16 | g.67940068G>T | CA396375568 | LCAT | c.1159C>A (p.Gln387Lys) c.162C>A c.897C>A (n.897C>A) | |
| 16 | g.67940069dup | CA623122722 | LCAT | c.1159dup (p.Gln387ProfsTer?) c.162dup c.897dup (n.897dup) | dbSNP gnomAD v2 |
| 16 | g.67940069G>A | CA496092782 | LCAT | c.1158C>T (p.Arg386=) c.161C>T c.896C>T (n.896C>T) | |
| 16 | g.67940069G>C | CA496092784 | LCAT | c.1158C>G (p.Arg386=) c.161C>G c.896C>G (n.896C>G) | |
| 16 | g.67940069G>T | CA496092786 | LCAT | c.1158C>A (p.Arg386=) c.161C>A c.896C>A (n.896C>A) | |
| 16 | g.67940070C>A | CA396375570 | LCAT | c.1157G>T (p.Arg386Leu) c.160G>T c.895G>T (n.895G>T) | |
| 16 | g.67940070C= | CA2229563192 | LCAT | c.1157G= (p.Arg386=) c.160G= c.895G= (n.895G=) | |
| 16 | g.67940070C>G | CA8120879 | LCAT | c.1157G>C (p.Arg386Pro) c.160G>C c.895G>C (n.895G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940070C>T | CA396375569 | LCAT | c.1157G>A (p.Arg386His) c.160G>A c.895G>A (n.895G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.67940071G>A | CA396375573 | LCAT | c.1156C>T (p.Arg386Cys) c.159C>T c.894C>T (n.894C>T) | gnomAD v4 |
| 16 | g.67940071G>C | CA396375571 | LCAT | c.1156C>G (p.Arg386Gly) c.159C>G c.894C>G (n.894C>G) | |
| 16 | g.67940071G>T | CA396375572 | LCAT | c.1156C>A (p.Arg386Ser) c.159C>A c.894C>A (n.894C>A) | |
| 16 | g.67940072G>A | CA496092804 | LCAT | c.1155C>T (p.Gly385=) c.158C>T c.893C>T (n.893C>T) | |
| 16 | g.67940072G>C | CA8120880 | LCAT | c.1155C>G (p.Gly385=) c.158C>G c.893C>G (n.893C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940072G= | CA2229563193 | LCAT | c.1155C= (p.Gly385=) c.158C= c.893C= (n.893C=) | |
| 16 | g.67940072G>T | CA496092810 | LCAT | c.1155C>A (p.Gly385=) c.158C>A c.893C>A (n.893C>A) | |
| 16 | g.67940072_67940082delinsGCCCTGCCACA | CA2229563194 | LCAT | c.1145_1155delinsTGTGGCAGGGC (p.Leu382=) c.156-8_158delinsTGTGGCAGGGC c.883_893delinsTGTGGCAGGGC (n.883_893delinsTGTGGCAGGGC) | |
| 16 | g.67940073C>A | CA396375574 | LCAT | c.1154G>T (p.Gly385Val) c.157G>T c.892G>T (n.892G>T) | gnomAD v4 |
| 16 | g.67940073C= | CA2229563195 | LCAT | c.1154G= (p.Gly385=) c.157G= c.892G= (n.892G=) | |
| 16 | g.67940073C>G | CA8120881 | LCAT | c.1154G>C (p.Gly385Ala) c.157G>C c.892G>C (n.892G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940073C>T | CA396375575 | LCAT | c.1154G>A (p.Gly385Asp) c.157G>A c.892G>A (n.892G>A) | gnomAD v4 |
| 16 | g.67940073_67940082del | CA919730844 | LCAT | c.1145_1154del (p.Leu382ProfsTer25) c.156-8_157del c.883_892del (n.883_892del) | dbSNP |
| 16 | g.67940074C>A | CA396375577 | LCAT | c.1153G>T (p.Gly385Cys) c.156G>T c.891G>T (n.891G>T) | |
| 16 | g.67940074C= | CA2229563196 | LCAT | c.1153G= (p.Gly385=) c.156G= c.891G= (n.891G=) | |
| 16 | g.67940074C>G | CA396375576 | LCAT | c.1153G>C (p.Gly385Arg) c.156G>C c.891G>C (n.891G>C) | dbSNP gnomAD v2 |
| 16 | g.67940074C>T | CA283160483 | LCAT | c.1153G>A (p.Gly385Ser) c.156G>A c.891G>A (n.891G>A) | dbSNP |
| 16 | g.67940075C>A | CA396375578 | LCAT | c.1152G>T (p.Gln384His) c.156-1G>T c.890G>T (n.890G>T) | |
| 16 | g.67940075C>G | CA396375579 | LCAT | c.1152G>C (p.Gln384His) c.156-1G>C c.890G>C (n.890G>C) | |
| 16 | g.67940075C>T | CA496092828 | LCAT | c.1152G>A (p.Gln384=) c.156-1G>A c.890G>A (n.890G>A) | |
| 16 | g.67940076T>A | CA396375580 | LCAT | c.1151A>T (p.Gln384Leu) c.156-2A>T c.889A>T (n.889A>T) | |
| 16 | g.67940076T>C | CA8120882 | LCAT | c.1151A>G (p.Gln384Arg) c.156-2A>G c.889A>G (n.889A>G) | dbSNP ExAC gnomAD v4 |
| 16 | g.67940076T>G | CA396375581 | LCAT | c.1151A>C (p.Gln384Pro) c.156-2A>C c.889A>C (n.889A>C) | |
| 16 | g.67940076T= | CA2229563197 | LCAT | c.1151A= (p.Gln384=) c.156-2A= c.889A= (n.889A=) | |
| 16 | g.67940077G>A | CA396375582 | LCAT | c.1150C>T (p.Gln384Ter) c.156-3C>T c.888C>T (n.888C>T) | |
| 16 | g.67940077G>C | CA8120883 | LCAT | c.1150C>G (p.Gln384Glu) c.156-3C>G c.888C>G (n.888C>G) | dbSNP ExAC |
| 16 | g.67940077G= | CA2229563198 | LCAT | c.1150C= (p.Gln384=) c.156-3C= c.888C= (n.888C=) | |
| 16 | g.67940077G>T | CA396375583 | LCAT | c.1150C>A (p.Gln384Lys) c.156-3C>A c.888C>A (n.888C>A) | |
| 16 | g.67940078C>A | CA396375584 | LCAT | c.1149G>T (p.Trp383Cys) c.156-4G>T c.887G>T (n.887G>T) | |
| 16 | g.67940078C= | CA2229563199 | LCAT | c.1149G= (p.Trp383=) c.156-4G= c.887G= (n.887G=) | |
| 16 | g.67940078C>G | CA283160485 | LCAT | c.1149G>C (p.Trp383Cys) c.156-4G>C c.887G>C (n.887G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940078C>T | CA396375585 | LCAT | c.1149G>A (p.Trp383Ter) c.156-4G>A c.887G>A (n.887G>A) | |
| 16 | g.67940079C>A | CA396375586 | LCAT | c.1148G>T (p.Trp383Leu) c.156-5G>T c.886G>T (n.886G>T) | |
| 16 | g.67940079C>G | CA396375587 | LCAT | c.1148G>C (p.Trp383Ser) c.156-5G>C c.886G>C (n.886G>C) | |
| 16 | g.67940079C>T | CA396375588 | LCAT | c.1148G>A (p.Trp383Ter) c.156-5G>A c.886G>A (n.886G>A) | |
| 16 | g.67940080A>C | CA396375589 | LCAT | c.1147T>G (p.Trp383Gly) c.156-6T>G c.885T>G (n.885T>G) | |
| 16 | g.67940080A>G | CA396375590 | LCAT | c.1147T>C (p.Trp383Arg) c.156-6T>C c.885T>C (n.885T>C) | |
| 16 | g.67940080A>T | CA396375591 | LCAT | c.1147T>A (p.Trp383Arg) c.156-6T>A c.885T>A (n.885T>A) | |
| 16 | g.67940081C>A | CA496092854 | LCAT | c.1146G>T (p.Leu382=) c.156-7G>T c.884G>T (n.884G>T) | |
| 16 | g.67940081C>G | CA496092855 | LCAT | c.1146G>C (p.Leu382=) c.156-7G>C c.884G>C (n.884G>C) | |
| 16 | g.67940081C>T | CA496092853 | LCAT | c.1146G>A (p.Leu382=) c.156-7G>A c.884G>A (n.884G>A) | gnomAD v4 |
| 16 | g.67940082A>C | CA396375592 | LCAT | c.1145T>G (p.Leu382Arg) c.156-8T>G c.883T>G (n.883T>G) | gnomAD v4 |
| 16 | g.67940082A>G | CA396375593 | LCAT | c.1145T>C (p.Leu382Pro) c.156-8T>C c.883T>C (n.883T>C) | |
| 16 | g.67940082A>T | CA396375594 | LCAT | c.1145T>A (p.Leu382Gln) c.156-8T>A c.883T>A (n.883T>A) | |
| 16 | g.67940083G>A | CA496092860 | LCAT | c.1144C>T (p.Leu382=) c.156-9C>T c.882C>T (n.882C>T) | |
| 16 | g.67940083G>C | CA396375595 | LCAT | c.1144C>G (p.Leu382Val) c.156-9C>G c.882C>G (n.882C>G) | |
| 16 | g.67940083G>T | CA396375596 | LCAT | c.1144C>A (p.Leu382Met) c.156-9C>A c.882C>A (n.882C>A) | |
| 16 | g.67940084G>A | CA496092866 | LCAT | c.1143C>T (p.Gly381=) c.156-10C>T c.881C>T (n.881C>T) | dbSNP |
| 16 | g.67940084G>C | CA496092865 | LCAT | c.1143C>G (p.Gly381=) c.156-10C>G c.881C>G (n.881C>G) | |
| 16 | g.67940084G>T | CA496092863 | LCAT | c.1143C>A (p.Gly381=) c.156-10C>A c.881C>A (n.881C>A) | |
| 16 | g.67940085C>A | CA396375597 | LCAT | c.1142G>T (p.Gly381Val) c.156-11G>T c.880G>T (n.880G>T) | |
| 16 | g.67940085C>G | CA396375598 | LCAT | c.1142G>C (p.Gly381Ala) c.156-11G>C c.880G>C (n.880G>C) | |
| 16 | g.67940085C>T | CA396375599 | LCAT | c.1142G>A (p.Gly381Asp) c.156-11G>A c.880G>A (n.880G>A) | gnomAD v4 |
| 16 | g.67940086C>A | CA396375600 | LCAT | c.1141G>T (p.Gly381Cys) c.156-12G>T c.879G>T (n.879G>T) | |
| 16 | g.67940086C>G | CA396375601 | LCAT | c.1141G>C (p.Gly381Arg) c.156-12G>C c.879G>C (n.879G>C) | |
| 16 | g.67940086C>T | CA396375602 | LCAT | c.1141G>A (p.Gly381Ser) c.156-12G>A c.879G>A (n.879G>A) | |
| 16 | g.67940087A>C | CA396375604 | LCAT | c.1140T>G (p.Cys380Trp) c.156-13T>G c.878T>G (n.878T>G) | |
| 16 | g.67940087A>G | CA496092874 | LCAT | c.1140T>C (p.Cys380=) c.156-13T>C c.878T>C (n.878T>C) | |
| 16 | g.67940087A>T | CA396375603 | LCAT | c.1140T>A (p.Cys380Ter) c.156-13T>A c.878T>A (n.878T>A) | |
| 16 | g.67940088C>A | CA396375605 | LCAT | c.1139G>T (p.Cys380Phe) c.156-14G>T c.877G>T (n.877G>T) | |
| 16 | g.67940088C= | CA2229563200 | LCAT | c.1139G= (p.Cys380=) c.156-14G= c.877G= (n.877G=) | |
| 16 | g.67940088C>G | CA396375606 | LCAT | c.1139G>C (p.Cys380Ser) c.156-14G>C c.877G>C (n.877G>C) | |
| 16 | g.67940088C>T | CA396375607 | LCAT | c.1139G>A (p.Cys380Tyr) c.156-14G>A c.877G>A (n.877G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940089A= | CA2229563201 | LCAT | c.1138T= (p.Cys380=) c.156-15T= c.876T= (n.876T=) | |
| 16 | g.67940089A>C | CA396375608 | LCAT | c.1138T>G (p.Cys380Gly) c.156-15T>G c.876T>G (n.876T>G) | |
| 16 | g.67940089A>G | CA8120884 | LCAT | c.1138T>C (p.Cys380Arg) c.156-15T>C c.876T>C (n.876T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940089A>T | CA396375609 | LCAT | c.1138T>A (p.Cys380Ser) c.156-15T>A c.876T>A (n.876T>A) | |
| 16 | g.67940090G>A | CA283160487 | LCAT | c.1137C>T (p.Leu379=) c.156-16C>T c.875C>T (n.875C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940090G>C | CA496092882 | LCAT | c.1137C>G (p.Leu379=) c.156-16C>G c.875C>G (n.875C>G) | |
| 16 | g.67940090G= | CA2229563202 | LCAT | c.1137C= (p.Leu379=) c.156-16C= c.875C= (n.875C=) | |
| 16 | g.67940090G>T | CA496092883 | LCAT | c.1137C>A (p.Leu379=) c.156-16C>A c.875C>A (n.875C>A) | |
| 16 | g.67940091A>C | CA396375610 | LCAT | c.1136T>G (p.Leu379Arg) c.156-17T>G c.874T>G (n.874T>G) | |
| 16 | g.67940091A>G | CA396375612 | LCAT | c.1136T>C (p.Leu379Pro) c.156-17T>C c.874T>C (n.874T>C) | |
| 16 | g.67940091A>T | CA396375611 | LCAT | c.1136T>A (p.Leu379His) c.156-17T>A c.874T>A (n.874T>A) | |
| 16 | g.67940092G>A | CA396375613 | LCAT | c.1135C>T (p.Leu379Phe) c.156-18C>T c.873C>T (n.873C>T) | dbSNP gnomAD v2 |
| 16 | g.67940092G>C | CA396375614 | LCAT | c.1135C>G (p.Leu379Val) c.156-18C>G c.873C>G (n.873C>G) | |
| 16 | g.67940092G= | CA2229563203 | LCAT | c.1135C= (p.Leu379=) c.156-18C= c.873C= (n.873C=) | |
| 16 | g.67940092G>T | CA396375615 | LCAT | c.1135C>A (p.Leu379Ile) c.156-18C>A c.873C>A (n.873C>A) | |
| 16 | g.67940093C>A | CA396375616 | LCAT | c.1134G>T (p.Glu378Asp) c.156-19G>T c.872G>T (n.872G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.67940093C= | CA2229563204 | LCAT | c.1134G= (p.Glu378=) c.156-19G= c.872G= (n.872G=) | |
| 16 | g.67940093C>G | CA396375617 | LCAT | c.1134G>C (p.Glu378Asp) c.156-19G>C c.872G>C (n.872G>C) | |
| 16 | g.67940093C>T | CA496383843 | LCAT | c.1134G>A (p.Glu378=) c.156-19G>A c.872G>A (n.872G>A) | |
| 16 | g.67940094T>A | CA396375618 | LCAT | c.1133A>T (p.Glu378Val) c.156-20A>T c.871A>T (n.871A>T) | |
| 16 | g.67940094T>C | CA396375619 | LCAT | c.1133A>G (p.Glu378Gly) c.156-20A>G c.871A>G (n.871A>G) | |
| 16 | g.67940094T>G | CA396375620 | LCAT | c.1133A>C (p.Glu378Ala) c.156-20A>C c.871A>C (n.871A>C) | |
| 16 | g.67940095C>A | CA396375621 | LCAT | c.1132G>T (p.Glu378Ter) c.156-21G>T c.870G>T (n.870G>T) | |
| 16 | g.67940095C= | CA2229563205 | LCAT | c.1132G= (p.Glu378=) c.156-21G= c.870G= (n.870G=) | |
| 16 | g.67940095C>G | CA396375622 | LCAT | c.1132G>C (p.Glu378Gln) c.156-21G>C c.870G>C (n.870G>C) | |
| 16 | g.67940095C>T | CA8120885 | LCAT | c.1132G>A (p.Glu378Lys) c.156-21G>A c.870G>A (n.870G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940096G>A | CA8120886 | LCAT | c.1131C>T (p.Thr377=) c.156-22C>T c.869C>T (n.869C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940096G>C | CA496383847 | LCAT | c.1131C>G (p.Thr377=) c.156-22C>G c.869C>G (n.869C>G) | gnomAD v4 |
| 16 | g.67940096G= | CA2229563206 | LCAT | c.1131C= (p.Thr377=) c.156-22C= c.869C= (n.869C=) | |
| 16 | g.67940096G>T | CA496383848 | LCAT | c.1131C>A (p.Thr377=) c.156-22C>A c.869C>A (n.869C>A) | |
| 16 | g.67940097G>A | CA396375624 | LCAT | c.1130C>T (p.Thr377Ile) c.156-23C>T c.868C>T (n.868C>T) | |
| 16 | g.67940097G>C | CA396375625 | LCAT | c.1130C>G (p.Thr377Ser) c.156-23C>G c.868C>G (n.868C>G) | |
| 16 | g.67940097G>T | CA396375623 | LCAT | c.1130C>A (p.Thr377Asn) c.156-23C>A c.868C>A (n.868C>A) | |
| 16 | g.67940098T>A | CA396375626 | LCAT | c.1129A>T (p.Thr377Ser) c.156-24A>T c.867A>T (n.867A>T) | |
| 16 | g.67940098T>C | CA396375627 | LCAT | c.1129A>G (p.Thr377Ala) c.156-24A>G c.867A>G (n.867A>G) | |
| 16 | g.67940098T>G | CA396375628 | LCAT | c.1129A>C (p.Thr377Pro) c.156-24A>C c.867A>C (n.867A>C) | |
| 16 | g.67940099G>A | CA496383852 | LCAT | c.1128C>T (p.Ser376=) c.156-25C>T c.866C>T (n.866C>T) | COSMIC |
| 16 | g.67940099G>C | CA396375629 | LCAT | c.1128C>G (p.Ser376Arg) c.156-25C>G c.866C>G (n.866C>G) | |
| 16 | g.67940099G>T | CA396375630 | LCAT | c.1128C>A (p.Ser376Arg) c.156-25C>A c.866C>A (n.866C>A) | |
| 16 | g.67940100C>A | CA396375633 | LCAT | c.1127G>T (p.Ser376Ile) c.156-26G>T c.865G>T (n.865G>T) | |
| 16 | g.67940100C>G | CA396375632 | LCAT | c.1127G>C (p.Ser376Thr) c.156-26G>C c.865G>C (n.865G>C) | |
| 16 | g.67940100C>T | CA396375631 | LCAT | c.1127G>A (p.Ser376Asn) c.156-26G>A c.865G>A (n.865G>A) | gnomAD v4 |
| 16 | g.67940101T>A | CA396375634 | LCAT | c.1126A>T (p.Ser376Cys) c.156-27A>T c.864A>T (n.864A>T) | |
| 16 | g.67940101T>C | CA396375635 | LCAT | c.1126A>G (p.Ser376Gly) c.156-27A>G c.864A>G (n.864A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67940101T>G | CA396375636 | LCAT | c.1126A>C (p.Ser376Arg) c.156-27A>C c.864A>C (n.864A>C) | |
| 16 | g.67940101T= | CA2229563207 | LCAT | c.1126A= (p.Ser376=) c.156-27A= c.864A= (n.864A=) | |
| 16 | g.67940106_67940107insCCCCCATGCGGG | CA2597452021 | LCAT | c.1126_1127insTGGGGGCCCGCA (p.Arg375_Ser376insMetGlyAlaArg) c.156-27_156-26insTGGGGGCCCGCA c.864_865insTGGGGGCCCGCA (n.864_865insTGGGGGCCCGCA) | gnomAD v3 gnomAD v4 |
| 16 | g.67940102G>A | CA496383856 | LCAT | c.1125C>T (p.Arg375=) c.156-28C>T c.863C>T (n.863C>T) | ClinVar |
| 16 | g.67940102G>C | CA496383854 | LCAT | c.1125C>G (p.Arg375=) c.156-28C>G c.863C>G (n.863C>G) | |
| 16 | g.67940102G>T | CA496383855 | LCAT | c.1125C>A (p.Arg375=) c.156-28C>A c.863C>A (n.863C>A) | |
| 16 | g.67940103C>A | CA396375637 | LCAT | c.1124G>T (p.Arg375Leu) c.156-29G>T c.862G>T (n.862G>T) | |
| 16 | g.67940103C= | CA2229563208 | LCAT | c.1124G= (p.Arg375=) c.156-29G= c.862G= (n.862G=) | |
| 16 | g.67940103C>G | CA396375638 | LCAT | c.1124G>C (p.Arg375Pro) c.156-29G>C c.862G>C (n.862G>C) | |
| 16 | g.67940103C>T | CA8120887 | LCAT | c.1124G>A (p.Arg375His) c.156-29G>A c.862G>A (n.862G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940104G>A | CA8120888 | LCAT | c.1123C>T (p.Arg375Cys) c.156-30C>T c.861C>T (n.861C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940104G>C | CA396375639 | LCAT | c.1123C>G (p.Arg375Gly) c.156-30C>G c.861C>G (n.861C>G) | |
| 16 | g.67940104G= | CA2229563209 | LCAT | c.1123C= (p.Arg375=) c.156-30C= c.861C= (n.861C=) | |
| 16 | g.67940104G>T | CA396375640 | LCAT | c.1123C>A (p.Arg375Ser) c.156-30C>A c.861C>A (n.861C>A) | |
| 16 | g.67940105G>A | CA496383859 | LCAT | c.1122C>T (p.Thr374=) c.156-31C>T c.860C>T (n.860C>T) | |
| 16 | g.67940105G>C | CA496383858 | LCAT | c.1122C>G (p.Thr374=) c.156-31C>G c.860C>G (n.860C>G) | gnomAD v4 |
| 16 | g.67940105G>T | CA496383857 | LCAT | c.1122C>A (p.Thr374=) c.156-31C>A c.860C>A (n.860C>A) | |
| 16 | g.67940106G>A | CA396375641 | LCAT | c.1121C>T (p.Thr374Ile) c.156-32C>T c.859C>T (n.859C>T) | |
| 16 | g.67940106G>C | CA396375642 | LCAT | c.1121C>G (p.Thr374Ser) c.156-32C>G c.859C>G (n.859C>G) | |
| 16 | g.67940106G>T | CA396375643 | LCAT | c.1121C>A (p.Thr374Asn) c.156-32C>A c.859C>A (n.859C>A) | |
| 16 | g.67940107T>A | CA396375644 | LCAT | c.1120A>T (p.Thr374Ser) c.156-33A>T c.858A>T (n.858A>T) | |
| 16 | g.67940107T>C | CA396375645 | LCAT | c.1120A>G (p.Thr374Ala) c.156-33A>G c.858A>G (n.858A>G) | |
| 16 | g.67940107T>G | CA396375646 | LCAT | c.1120A>C (p.Thr374Pro) c.156-33A>C c.858A>C (n.858A>C) | dbSNP gnomAD v2 |
| 16 | g.67940107T= | CA2229563210 | LCAT | c.1120A= (p.Thr374=) c.156-33A= c.858A= (n.858A=) | |
| 16 | g.67940108C>A | CA496383860 | LCAT | c.1119G>T (p.Ala373=) c.156-34G>T c.857G>T (n.857G>T) | gnomAD v4 |
| 16 | g.67940108C= | CA2229563211 | LCAT | c.1119G= (p.Ala373=) c.156-34G= c.857G= (n.857G=) | |
| 16 | g.67940108C>G | CA496383861 | LCAT | c.1119G>C (p.Ala373=) c.156-34G>C c.857G>C (n.857G>C) | |
| 16 | g.67940108C>T | CA283160525 | LCAT | c.1119G>A (p.Ala373=) c.156-34G>A c.857G>A (n.857G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940109G>A | CA8120889 | LCAT | c.1118C>T (p.Ala373Val) c.156-35C>T c.856C>T (n.856C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.67940109G>C | CA396375647 | LCAT | c.1118C>G (p.Ala373Gly) c.156-35C>G c.856C>G (n.856C>G) | |
| 16 | g.67940109G= | CA2229563212 | LCAT | c.1118C= (p.Ala373=) c.156-35C= c.856C= (n.856C=) | |
| 16 | g.67940109G>T | CA396375648 | LCAT | c.1118C>A (p.Ala373Glu) c.156-35C>A c.856C>A (n.856C>A) | |
| 16 | g.67940110C>A | CA396375649 | LCAT | c.1117G>T (p.Ala373Ser) c.156-36G>T c.855G>T (n.855G>T) | |
| 16 | g.67940110C>G | CA396375650 | LCAT | c.1117G>C (p.Ala373Pro) c.156-36G>C c.855G>C (n.855G>C) | |
| 16 | g.67940110C>T | CA396375651 | LCAT | c.1117G>A (p.Ala373Thr) c.156-36G>A c.855G>A (n.855G>A) | |
| 16 | g.67940112_67940114del | CA2633850710 | LCAT | c.1115_1117del (p.Val372del) c.156-38_156-36del c.853_855del (n.853_855del) | gnomAD v4 |
| 16 | g.67940111C>A | CA496383862 | LCAT | c.1116G>T (p.Val372=) c.156-37G>T c.854G>T (n.854G>T) | |
| 16 | g.67940111C>G | CA496383863 | LCAT | c.1116G>C (p.Val372=) c.156-37G>C c.854G>C (n.854G>C) | |
| 16 | g.67940111C>T | CA496383864 | LCAT | c.1116G>A (p.Val372=) c.156-37G>A c.854G>A (n.854G>A) | |
| 16 | g.67940112A>C | CA396375654 | LCAT | c.1115T>G (p.Val372Gly) c.156-38T>G c.853T>G (n.853T>G) | |
| 16 | g.67940112A>G | CA396375652 | LCAT | c.1115T>C (p.Val372Ala) c.156-38T>C c.853T>C (n.853T>C) | gnomAD v4 |
| 16 | g.67940112A>T | CA396375653 | LCAT | c.1115T>A (p.Val372Glu) c.156-38T>A c.853T>A (n.853T>A) | |
| 16 | g.67940113C>A | CA396375655 | LCAT | c.1114G>T (p.Val372Leu) c.156-39G>T c.852G>T (n.852G>T) | |
| 16 | g.67940113C>G | CA396375656 | LCAT | c.1114G>C (p.Val372Leu) c.156-39G>C c.852G>C (n.852G>C) | |
| 16 | g.67940113C>T | CA396375657 | LCAT | c.1114G>A (p.Val372Met) c.156-39G>A c.852G>A (n.852G>A) | |
| 16 | g.67940114C>A | CA496383866 | LCAT | c.1113G>T (p.Thr371=) c.156-40G>T c.851G>T (n.851G>T) | |
| 16 | g.67940114C= | CA2229563213 | LCAT | c.1113G= (p.Thr371=) c.156-40G= c.851G= (n.851G=) | |
| 16 | g.67940114C>G | CA496383867 | LCAT | c.1113G>C (p.Thr371=) c.156-40G>C c.851G>C (n.851G>C) | gnomAD v4 |
| 16 | g.67940114C>T | CA8120890 | LCAT | c.1113G>A (p.Thr371=) c.156-40G>A c.851G>A (n.851G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940115G>A | CA116420 | LCAT | c.1112C>T (p.Thr371Met) c.156-41C>T c.850C>T (n.850C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940115G>C | CA396375658 | LCAT | c.1112C>G (p.Thr371Arg) c.156-41C>G c.850C>G (n.850C>G) | |
| 16 | g.67940115G= | CA2229563214 | LCAT | c.1112C= (p.Thr371=) c.156-41C= c.850C= (n.850C=) | |
| 16 | g.67940115G>T | CA396375659 | LCAT | c.1112C>A (p.Thr371Lys) c.156-41C>A c.850C>A (n.850C>A) | gnomAD v4 |
| 16 | g.67940116T>A | CA396375662 | LCAT | c.1111A>T (p.Thr371Ser) c.156-42A>T c.849A>T (n.849A>T) | |
| 16 | g.67940116T>C | CA396375660 | LCAT | c.1111A>G (p.Thr371Ala) c.156-42A>G c.849A>G (n.849A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67940116T>G | CA396375661 | LCAT | c.1111A>C (p.Thr371Pro) c.156-42A>C c.849A>C (n.849A>C) | |
| 16 | g.67940116T= | CA2229563215 | LCAT | c.1111A= (p.Thr371=) c.156-42A= c.849A= (n.849A=) | |
| 16 | g.67940117G>A | CA496383869 | LCAT | c.1110C>T (p.Asp370=) c.156-43C>T c.848C>T (n.848C>T) | |
| 16 | g.67940117G>C | CA396375663 | LCAT | c.1110C>G (p.Asp370Glu) c.156-43C>G c.848C>G (n.848C>G) | |
| 16 | g.67940117G>T | CA396375664 | LCAT | c.1110C>A (p.Asp370Glu) c.156-43C>A c.848C>A (n.848C>A) | |
| 16 | g.67940117_67940120delinsGTCA | CA2229563216 | LCAT | c.1107_1110delinsTGAC (p.Asp369=) c.156-46_156-43delinsTGAC c.845_848delinsTGAC (n.845_848delinsTGAC) | |
| 16 | g.67940118T>A | CA396375665 | LCAT | c.1109A>T (p.Asp370Val) c.156-44A>T c.847A>T (n.847A>T) | |
| 16 | g.67940118T>C | CA396375666 | LCAT | c.1109A>G (p.Asp370Gly) c.156-44A>G c.847A>G (n.847A>G) | |
| 16 | g.67940118T>G | CA396375667 | LCAT | c.1109A>C (p.Asp370Ala) c.156-44A>C c.847A>C (n.847A>C) | |
| 16 | g.67940121_67940123del | CA623122337 | LCAT | c.1107_1109del (p.Asp370del) c.156-46_156-44del c.845_847del (n.845_847del) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.67940119C>A | CA396375668 | LCAT | c.1108G>T (p.Asp370Tyr) c.156-45G>T c.846G>T (n.846G>T) | |
| 16 | g.67940119C= | CA2229563217 | LCAT | c.1108G= (p.Asp370=) c.156-45G= c.846G= (n.846G=) | |
| 16 | g.67940119C>G | CA396375670 | LCAT | c.1108G>C (p.Asp370His) c.156-45G>C c.846G>C (n.846G>C) | |
| 16 | g.67940119C>T | CA396375669 | LCAT | c.1108G>A (p.Asp370Asn) c.156-45G>A c.846G>A (n.846G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.67940120A>C | CA396375671 | LCAT | c.1107T>G (p.Asp369Glu) c.156-46T>G c.845T>G (n.845T>G) | |
| 16 | g.67940120A>G | CA496383871 | LCAT | c.1107T>C (p.Asp369=) c.156-46T>C c.845T>C (n.845T>C) | |
| 16 | g.67940120A>T | CA396375672 | LCAT | c.1107T>A (p.Asp369Glu) c.156-46T>A c.845T>A (n.845T>A) | |
| 16 | g.67940121T>A | CA396375673 | LCAT | c.1106A>T (p.Asp369Val) c.156-47A>T c.844A>T (n.844A>T) | |
| 16 | g.67940121T>C | CA396375674 | LCAT | c.1106A>G (p.Asp369Gly) c.156-47A>G c.844A>G (n.844A>G) | gnomAD v4 |
| 16 | g.67940121T>G | CA396375675 | LCAT | c.1106A>C (p.Asp369Ala) c.156-47A>C c.844A>C (n.844A>C) | |
| 16 | g.67940121_67940124delinsTCAC | CA2229563218 | LCAT | c.1103_1106delinsGTGA (p.Gly368=) c.156-50_156-47delinsGTGA c.841_844delinsGTGA (n.841_844delinsGTGA) | |
| 16 | g.67940122C>A | CA396375676 | LCAT | c.1105G>T (p.Asp369Tyr) c.156-48G>T c.843G>T (n.843G>T) | |
| 16 | g.67940122C>G | CA396375677 | LCAT | c.1105G>C (p.Asp369His) c.156-48G>C c.843G>C (n.843G>C) | |
| 16 | g.67940122C>T | CA396375678 | LCAT | c.1105G>A (p.Asp369Asn) c.156-48G>A c.843G>A (n.843G>A) | gnomAD v4 |
| 16 | g.67940124_67940126del | CA8120891 | LCAT | c.1103_1105del (p.Gly368del) c.156-50_156-48del c.841_843del (n.841_843del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940123A>C | CA496383877 | LCAT | c.1104T>G (p.Gly368=) c.156-49T>G c.842T>G (n.842T>G) | |
| 16 | g.67940123A>G | CA496383876 | LCAT | c.1104T>C (p.Gly368=) c.156-49T>C c.842T>C (n.842T>C) | dbSNP gnomAD v4 |
| 16 | g.67940123A>T | CA496383875 | LCAT | c.1104T>A (p.Gly368=) c.156-49T>A c.842T>A (n.842T>A) | |
| 16 | g.67940124C>A | CA8120892 | LCAT | c.1103G>T (p.Gly368Val) c.156-50G>T c.841G>T (n.841G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940124C= | CA2229563219 | LCAT | c.1103G= (p.Gly368=) c.156-50G= c.841G= (n.841G=) | |
| 16 | g.67940124C>G | CA396375679 | LCAT | c.1103G>C (p.Gly368Ala) c.156-50G>C c.841G>C (n.841G>C) | |
| 16 | g.67940124C>T | CA396375680 | LCAT | c.1103G>A (p.Gly368Asp) c.156-50G>A c.841G>A (n.841G>A) | |
| 16 | g.67940125C>A | CA396375681 | LCAT | c.1102G>T (p.Gly368Cys) c.156-51G>T c.840G>T (n.840G>T) | |
| 16 | g.67940125C= | CA2229563220 | LCAT | c.1102G= (p.Gly368=) c.156-51G= c.840G= (n.840G=) | |
| 16 | g.67940125C>G | CA396375682 | LCAT | c.1102G>C (p.Gly368Arg) c.156-51G>C c.840G>C (n.840G>C) | |
| 16 | g.67940125C>T | CA8120893 | LCAT | c.1102G>A (p.Gly368Ser) c.156-51G>A c.840G>A (n.840G>A) | dbSNP ExAC gnomAD v4 |
| 16 | g.67940126A= | CA2229563221 | LCAT | c.1101T= (p.Asp367=) c.156-52T= c.839T= (n.839T=) | |
| 16 | g.67940126A>C | CA396375683 | LCAT | c.1101T>G (p.Asp367Glu) c.156-52T>G c.839T>G (n.839T>G) | |
| 16 | g.67940126A>G | CA8120894 | LCAT | c.1101T>C (p.Asp367=) c.156-52T>C c.839T>C (n.839T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940126A>T | CA396375684 | LCAT | c.1101T>A (p.Asp367Glu) c.156-52T>A c.839T>A (n.839T>A) | |
| 16 | g.67940127T>A | CA396375685 | LCAT | c.1100A>T (p.Asp367Val) c.156-53A>T c.838A>T (n.838A>T) | |
| 16 | g.67940127T>C | CA396375686 | LCAT | c.1100A>G (p.Asp367Gly) c.156-53A>G c.838A>G (n.838A>G) | |
| 16 | g.67940127T>G | CA396375687 | LCAT | c.1100A>C (p.Asp367Ala) c.156-53A>C c.838A>C (n.838A>C) | |
| 16 | g.67940128C>A | CA396375688 | LCAT | c.1099G>T (p.Asp367Tyr) c.156-54G>T c.837G>T (n.837G>T) | |
| 16 | g.67940128C>G | CA396375689 | LCAT | c.1099G>C (p.Asp367His) c.156-54G>C c.837G>C (n.837G>C) | COSMIC |
| 16 | g.67940128C>T | CA396375690 | LCAT | c.1099G>A (p.Asp367Asn) c.156-54G>A c.837G>A (n.837G>A) | gnomAD v4 |
| 16 | g.67940129C>A | CA396375691 | LCAT | c.1098G>T (p.Glu366Asp) c.156-55G>T c.836G>T (n.836G>T) | |
| 16 | g.67940129C= | CA2229563222 | LCAT | c.1098G= (p.Glu366=) c.156-55G= c.836G= (n.836G=) | |
| 16 | g.67940129C>G | CA396375692 | LCAT | c.1098G>C (p.Glu366Asp) c.156-55G>C c.836G>C (n.836G>C) | |
| 16 | g.67940129C>T | CA496383884 | LCAT | c.1098G>A (p.Glu366=) c.156-55G>A c.836G>A (n.836G>A) | ClinVar dbSNP |
| 16 | g.67940130T>A | CA396375693 | LCAT | c.1097A>T (p.Glu366Val) c.156-56A>T c.835A>T (n.835A>T) | |
| 16 | g.67940130T>C | CA396375694 | LCAT | c.1097A>G (p.Glu366Gly) c.156-56A>G c.835A>G (n.835A>G) | gnomAD v4 |
| 16 | g.67940130T>G | CA396375695 | LCAT | c.1097A>C (p.Glu366Ala) c.156-56A>C c.835A>C (n.835A>C) | |
| 16 | g.67940131C>A | CA396375697 | LCAT | c.1096G>T (p.Glu366Ter) c.156-57G>T c.834G>T (n.834G>T) | |
| 16 | g.67940131C= | CA2229563223 | LCAT | c.1096G= (p.Glu366=) c.156-57G= c.834G= (n.834G=) | |
| 16 | g.67940131C>G | CA396375696 | LCAT | c.1096G>C (p.Glu366Gln) c.156-57G>C c.834G>C (n.834G>C) | |
| 16 | g.67940131C>T | CA8120895 | LCAT | c.1096G>A (p.Glu366Lys) c.156-57G>A c.834G>A (n.834G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940132A= | CA2229563224 | LCAT | c.1095T= (p.Tyr365=) c.156-58T= c.833T= (n.833T=) | |
| 16 | g.67940132A>C | CA396375698 | LCAT | c.1095T>G (p.Tyr365Ter) c.156-58T>G c.833T>G (n.833T>G) | |
| 16 | g.67940132A>G | CA496383888 | LCAT | c.1095T>C (p.Tyr365=) c.156-58T>C c.833T>C (n.833T>C) | dbSNP |
| 16 | g.67940132A>T | CA396375699 | LCAT | c.1095T>A (p.Tyr365Ter) c.156-58T>A c.833T>A (n.833T>A) | |
| 16 | g.67940133del | CA2576033439 | LCAT | c.1094del (p.Tyr365LeufsTer?) c.156-59del c.832del (n.832del) | |
| 16 | g.67940133T>A | CA396375700 | LCAT | c.1094A>T (p.Tyr365Phe) c.156-59A>T c.832A>T (n.832A>T) | |
| 16 | g.67940133T>C | CA396375701 | LCAT | c.1094A>G (p.Tyr365Cys) c.156-59A>G c.832A>G (n.832A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67940133T>G | CA396375702 | LCAT | c.1094A>C (p.Tyr365Ser) c.156-59A>C c.832A>C (n.832A>C) | |
| 16 | g.67940133T= | CA2229563225 | LCAT | c.1094A= (p.Tyr365=) c.156-59A= c.832A= (n.832A=) | |
| 16 | g.67940134A= | CA2229563226 | LCAT | c.1093T= (p.Tyr365=) c.156-60T= c.831T= (n.831T=) | |
| 16 | g.67940134A>C | CA396375703 | LCAT | c.1093T>G (p.Tyr365Asp) c.156-60T>G c.831T>G (n.831T>G) | |
| 16 | g.67940134A>G | CA8120896 | LCAT | c.1093T>C (p.Tyr365His) c.156-60T>C c.831T>C (n.831T>C) | dbSNP ExAC gnomAD v4 |
| 16 | g.67940134A>T | CA396375704 | LCAT | c.1093T>A (p.Tyr365Asn) c.156-60T>A c.831T>A (n.831T>A) | |
| 16 | g.67940135G>A | CA496383891 | LCAT | c.1092C>T (p.Leu364=) c.156-61C>T c.830C>T (n.830C>T) | |
| 16 | g.67940135G>C | CA496383892 | LCAT | c.1092C>G (p.Leu364=) c.156-61C>G c.830C>G (n.830C>G) | |
| 16 | g.67940135G>T | CA496383893 | LCAT | c.1092C>A (p.Leu364=) c.156-61C>A c.830C>A (n.830C>A) | |
| 16 | g.67940136A>C | CA396375705 | LCAT | c.1091T>G (p.Leu364Arg) c.156-62T>G c.829T>G (n.829T>G) | |
| 16 | g.67940136A>G | CA396375706 | LCAT | c.1091T>C (p.Leu364Pro) c.156-62T>C c.829T>C (n.829T>C) | |
| 16 | g.67940136A>T | CA396375707 | LCAT | c.1091T>A (p.Leu364His) c.156-62T>A c.829T>A (n.829T>A) | |
| 16 | g.67940137G>A | CA396375709 | LCAT | c.1090C>T (p.Leu364Phe) c.156-63C>T c.828C>T (n.828C>T) | gnomAD v4 |
| 16 | g.67940137G>C | CA396375710 | LCAT | c.1090C>G (p.Leu364Val) c.156-63C>G c.828C>G (n.828C>G) | |
| 16 | g.67940137G>T | CA396375708 | LCAT | c.1090C>A (p.Leu364Ile) c.156-63C>A c.828C>A (n.828C>A) | |
| 16 | g.67940138C>A | CA496383896 | LCAT | c.1089G>T (p.Val363=) c.156-64G>T c.827G>T (n.827G>T) | |
| 16 | g.67940138C>G | CA496383897 | LCAT | c.1089G>C (p.Val363=) c.156-64G>C c.827G>C (n.827G>C) | gnomAD v4 |
| 16 | g.67940138C>T | CA496383898 | LCAT | c.1089G>A (p.Val363=) c.156-64G>A c.827G>A (n.827G>A) | |
| 16 | g.67940139A>C | CA396375711 | LCAT | c.1088T>G (p.Val363Gly) c.156-65T>G c.826T>G (n.826T>G) | |
| 16 | g.67940139A>G | CA396375712 | LCAT | c.1088T>C (p.Val363Ala) c.156-65T>C c.826T>C (n.826T>C) | |
| 16 | g.67940139A>T | CA396375713 | LCAT | c.1088T>A (p.Val363Glu) c.156-65T>A c.826T>A (n.826T>A) | ClinVar |
| 16 | g.67940140C>A | CA396375714 | LCAT | c.1087G>T (p.Val363Leu) c.156-66G>T c.825G>T (n.825G>T) | |
| 16 | g.67940140C>G | CA396375715 | LCAT | c.1087G>C (p.Val363Leu) c.156-66G>C c.825G>C (n.825G>C) | |
| 16 | g.67940140C>T | CA396375716 | LCAT | c.1087G>A (p.Val363Met) c.156-66G>A c.825G>A (n.825G>A) | |
| 16 | g.67940141A= | CA2229563227 | LCAT | c.1086T= (p.Gly362=) c.156-67T= c.824T= (n.824T=) | |
| 16 | g.67940141A>C | CA496383902 | LCAT | c.1086T>G (p.Gly362=) c.156-67T>G c.824T>G (n.824T>G) | dbSNP |
| 16 | g.67940141A>G | CA496383903 | LCAT | c.1086T>C (p.Gly362=) c.156-67T>C c.824T>C (n.824T>C) | |
| 16 | g.67940141A>T | CA496383904 | LCAT | c.1086T>A (p.Gly362=) c.156-67T>A c.824T>A (n.824T>A) | |
| 16 | g.67940142C>A | CA396375717 | LCAT | c.1085G>T (p.Gly362Val) c.156-68G>T c.823G>T (n.823G>T) | dbSNP |
| 16 | g.67940142C= | CA2229563228 | LCAT | c.1085G= (p.Gly362=) c.156-68G= c.823G= (n.823G=) | |
| 16 | g.67940142C>G | CA8120897 | LCAT | c.1085G>C (p.Gly362Ala) c.156-68G>C c.823G>C (n.823G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940142C>T | CA396375718 | LCAT | c.1085G>A (p.Gly362Asp) c.156-68G>A c.823G>A (n.823G>A) | ClinVar dbSNP |
| 16 | g.67940143C>A | CA396375719 | LCAT | c.1084G>T (p.Gly362Cys) c.156-69G>T c.822G>T (n.822G>T) | |
| 16 | g.67940143C>G | CA396375720 | LCAT | c.1084G>C (p.Gly362Arg) c.156-69G>C c.822G>C (n.822G>C) | |
| 16 | g.67940143C>T | CA396375721 | LCAT | c.1084G>A (p.Gly362Ser) c.156-69G>A c.822G>A (n.822G>A) | ClinVar |
| 16 | g.67940144C>A | CA496383910 | LCAT | c.1083G>T (p.Val361=) c.156-70G>T c.821G>T (n.821G>T) | |
| 16 | g.67940144C= | CA2229563229 | LCAT | c.1083G= (p.Val361=) c.156-70G= c.821G= (n.821G=) | |
| 16 | g.67940144C>G | CA496383908 | LCAT | c.1083G>C (p.Val361=) c.156-70G>C c.821G>C (n.821G>C) | |
| 16 | g.67940144C>T | CA496383909 | LCAT | c.1083G>A (p.Val361=) c.156-70G>A c.821G>A (n.821G>A) | ClinVar dbSNP |
| 16 | g.67940145A>C | CA396375723 | LCAT | c.1082T>G (p.Val361Gly) c.156-71T>G c.820T>G (n.820T>G) | |
| 16 | g.67940145A>G | CA396375724 | LCAT | c.1082T>C (p.Val361Ala) c.156-71T>C c.820T>C (n.820T>C) | |
| 16 | g.67940145A>T | CA396375722 | LCAT | c.1082T>A (p.Val361Glu) c.156-71T>A c.820T>A (n.820T>A) | |
| 16 | g.67940146C>A | CA396375725 | LCAT | c.1081G>T (p.Val361Leu) c.156-72G>T c.819G>T (n.819G>T) | |
| 16 | g.67940146C>G | CA396375726 | LCAT | c.1081G>C (p.Val361Leu) c.156-72G>C c.819G>C (n.819G>C) | gnomAD v4 |
| 16 | g.67940146C>T | CA396375727 | LCAT | c.1081G>A (p.Val361Met) c.156-72G>A c.819G>A (n.819G>A) | gnomAD v4 |
| 16 | g.67940147A>C | CA496383914 | LCAT | c.1080T>G (p.Pro360=) c.156-73T>G c.818T>G (n.818T>G) | gnomAD v4 |
| 16 | g.67940147A>G | CA496383915 | LCAT | c.1080T>C (p.Pro360=) c.156-73T>C c.818T>C (n.818T>C) | gnomAD v4 |
| 16 | g.67940147A>T | CA496383916 | LCAT | c.1080T>A (p.Pro360=) c.156-73T>A c.818T>A (n.818T>A) | |
| 16 | g.67940148G>A | CA396375728 | LCAT | c.1079C>T (p.Pro360Leu) c.156-74C>T c.817C>T (n.817C>T) | |
| 16 | g.67940148G>C | CA396375729 | LCAT | c.1079C>G (p.Pro360Arg) c.156-74C>G c.817C>G (n.817C>G) | |
| 16 | g.67940148G>T | CA396375730 | LCAT | c.1079C>A (p.Pro360His) c.156-74C>A c.817C>A (n.817C>A) | |
| 16 | g.67940150del | CA2633850746 | LCAT | c.1079del (p.Pro360LeufsTer?) c.156-74del c.817del (n.817del) | gnomAD v4 |
| 16 | g.67940149G>A | CA396375732 | LCAT | c.1078C>T (p.Pro360Ser) c.156-75C>T c.816C>T (n.816C>T) | |
| 16 | g.67940149G>C | CA396375731 | LCAT | c.1078C>G (p.Pro360Ala) c.156-75C>G c.816C>G (n.816C>G) | |
| 16 | g.67940149G= | CA2229563230 | LCAT | c.1078C= (p.Pro360=) c.156-75C= c.816C= (n.816C=) | |
| 16 | g.67940149G>T | CA8120898 | LCAT | c.1078C>A (p.Pro360Thr) c.156-75C>A c.816C>A (n.816C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940150G>A | CA496383919 | LCAT | c.1077C>T (p.Asp359=) c.156-76C>T c.815C>T (n.815C>T) | ClinVar |
| 16 | g.67940150G>C | CA396375733 | LCAT | c.1077C>G (p.Asp359Glu) c.156-76C>G c.815C>G (n.815C>G) | |
| 16 | g.67940150G>T | CA396375734 | LCAT | c.1077C>A (p.Asp359Glu) c.156-76C>A c.815C>A (n.815C>A) | |
| 16 | g.67940151T>A | CA396375735 | LCAT | c.1076A>T (p.Asp359Val) c.156-77A>T c.814A>T (n.814A>T) | |
| 16 | g.67940151T>C | CA396375736 | LCAT | c.1076A>G (p.Asp359Gly) c.156-77A>G c.814A>G (n.814A>G) | |
| 16 | g.67940151T>G | CA396375737 | LCAT | c.1076A>C (p.Asp359Ala) c.156-77A>C c.814A>C (n.814A>C) | |
| 16 | g.67940152C>A | CA396375738 | LCAT | c.1075G>T (p.Asp359Tyr) c.156-78G>T c.813G>T (n.813G>T) | |
| 16 | g.67940152C>G | CA396375740 | LCAT | c.1075G>C (p.Asp359His) c.156-78G>C c.813G>C (n.813G>C) | |
| 16 | g.67940152C>T | CA396375739 | LCAT | c.1075G>A (p.Asp359Asn) c.156-78G>A c.813G>A (n.813G>A) | |
| 16 | g.67940153C>A | CA496383921 | LCAT | c.1074G>T (p.Thr358=) c.156-79G>T c.812G>T (n.812G>T) | |
| 16 | g.67940153C= | CA2229563231 | LCAT | c.1074G= (p.Thr358=) c.156-79G= c.812G= (n.812G=) | |
| 16 | g.67940153C>G | CA496383922 | LCAT | c.1074G>C (p.Thr358=) c.156-79G>C c.812G>C (n.812G>C) | gnomAD v4 |
| 16 | g.67940153C>T | CA8120899 | LCAT | c.1074G>A (p.Thr358=) c.156-79G>A c.812G>A (n.812G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940154G>A | CA8120900 | LCAT | c.1073C>T (p.Thr358Met) c.156-80C>T c.811C>T (n.811C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940154G>C | CA396375741 | LCAT | c.1073C>G (p.Thr358Arg) c.156-80C>G c.811C>G (n.811C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940154G= | CA2229563232 | LCAT | c.1073C= (p.Thr358=) c.156-80C= c.811C= (n.811C=) | |
| 16 | g.67940154G>T | CA396375742 | LCAT | c.1073C>A (p.Thr358Lys) c.156-80C>A c.811C>A (n.811C>A) | |
| 16 | g.67940155T>A | CA396375743 | LCAT | c.1072A>T (p.Thr358Ser) c.156-81A>T c.810A>T (n.810A>T) | |
| 16 | g.67940155T>C | CA396375744 | LCAT | c.1072A>G (p.Thr358Ala) c.156-81A>G c.810A>G (n.810A>G) | dbSNP |
| 16 | g.67940155T>G | CA396375745 | LCAT | c.1072A>C (p.Thr358Pro) c.156-81A>C c.810A>C (n.810A>C) | |
| 16 | g.67940155T= | CA2229563233 | LCAT | c.1072A= (p.Thr358=) c.156-81A= c.810A= (n.810A=) | |
| 16 | g.67940156G>A | CA283160616 | LCAT | c.1071C>T (p.Tyr357=) c.156-82C>T c.809C>T (n.809C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940156G>C | CA396375746 | LCAT | c.1071C>G (p.Tyr357Ter) c.156-82C>G c.809C>G (n.809C>G) | |
| 16 | g.67940156G= | CA2229563234 | LCAT | c.1071C= (p.Tyr357=) c.156-82C= c.809C= (n.809C=) | |
| 16 | g.67940156G>T | CA396375747 | LCAT | c.1071C>A (p.Tyr357Ter) c.156-82C>A c.809C>A (n.809C>A) | |
| 16 | g.67940157T>A | CA396375748 | LCAT | c.1070A>T (p.Tyr357Phe) c.156-83A>T c.808A>T (n.808A>T) | gnomAD v4 |
| 16 | g.67940157T>C | CA396375749 | LCAT | c.1070A>G (p.Tyr357Cys) c.156-83A>G c.808A>G (n.808A>G) | |
| 16 | g.67940157T>G | CA396375750 | LCAT | c.1070A>C (p.Tyr357Ser) c.156-83A>C c.808A>C (n.808A>C) | |
| 16 | g.67940158A>C | CA396375751 | LCAT | c.1069T>G (p.Tyr357Asp) c.156-84T>G c.807T>G (n.807T>G) | |
| 16 | g.67940158A>G | CA396375752 | LCAT | c.1069T>C (p.Tyr357His) c.156-84T>C c.807T>C (n.807T>C) | |
| 16 | g.67940158A>T | CA396375753 | LCAT | c.1069T>A (p.Tyr357Asn) c.156-84T>A c.807T>A (n.807T>A) | |
| 16 | g.67940159G>A | CA283160630 | LCAT | c.1068C>T (p.Pro356=) c.156-85C>T c.806C>T (n.806C>T) | ClinVar dbSNP gnomAD v4 |
| 16 | g.67940159G>C | CA496383930 | LCAT | c.1068C>G (p.Pro356=) c.156-85C>G c.806C>G (n.806C>G) | |
| 16 | g.67940159G= | CA2229563235 | LCAT | c.1068C= (p.Pro356=) c.156-85C= c.806C= (n.806C=) | |
| 16 | g.67940159G>T | CA496383931 | LCAT | c.1068C>A (p.Pro356=) c.156-85C>A c.806C>A (n.806C>A) | |
| 16 | g.67940160G>A | CA396375754 | LCAT | c.1067C>T (p.Pro356Leu) c.156-86C>T c.805C>T (n.805C>T) | dbSNP |
| 16 | g.67940160G>C | CA396375755 | LCAT | c.1067C>G (p.Pro356Arg) c.156-86C>G c.805C>G (n.805C>G) | |
| 16 | g.67940160G= | CA2229563236 | LCAT | c.1067C= (p.Pro356=) c.156-86C= c.805C= (n.805C=) | |
| 16 | g.67940160G>T | CA396375756 | LCAT | c.1067C>A (p.Pro356His) c.156-86C>A c.805C>A (n.805C>A) | |
| 16 | g.67940161G>A | CA8120901 | LCAT | c.1066C>T (p.Pro356Ser) c.156-87C>T c.804C>T (n.804C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.67940161G>C | CA396375757 | LCAT | c.1066C>G (p.Pro356Ala) c.156-87C>G c.804C>G (n.804C>G) | |
| 16 | g.67940161G= | CA2229563237 | LCAT | c.1066C= (p.Pro356=) c.156-87C= c.804C= (n.804C=) | |
| 16 | g.67940161G>T | CA396375758 | LCAT | c.1066C>A (p.Pro356Thr) c.156-87C>A c.804C>A (n.804C>A) | |
| 16 | g.67940162G>A | CA496383933 | LCAT | c.1065C>T (p.Phe355=) c.156-88C>T c.803C>T (n.803C>T) | |
| 16 | g.67940162G>C | CA396375759 | LCAT | c.1065C>G (p.Phe355Leu) c.156-88C>G c.803C>G (n.803C>G) | |
| 16 | g.67940162G>T | CA396375760 | LCAT | c.1065C>A (p.Phe355Leu) c.156-88C>A c.803C>A (n.803C>A) | |
| 16 | g.67940163A= | CA2229563238 | LCAT | c.1064T= (p.Phe355=) c.156-89T= c.802T= (n.802T=) | |
| 16 | g.67940163A>C | CA396375761 | LCAT | c.1064T>G (p.Phe355Cys) c.156-89T>G c.802T>G (n.802T>G) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67940163A>G | CA396375762 | LCAT | c.1064T>C (p.Phe355Ser) c.156-89T>C c.802T>C (n.802T>C) | |
| 16 | g.67940163A>T | CA396375763 | LCAT | c.1064T>A (p.Phe355Tyr) c.156-89T>A c.802T>A (n.802T>A) | |
| 16 | g.67940164A>C | CA396375764 | LCAT | c.1063T>G (p.Phe355Val) c.156-90T>G c.801T>G (n.801T>G) | |
| 16 | g.67940164A>G | CA396375765 | LCAT | c.1063T>C (p.Phe355Leu) c.156-90T>C c.801T>C (n.801T>C) | |
| 16 | g.67940164A>T | CA396375766 | LCAT | c.1063T>A (p.Phe355Ile) c.156-90T>A c.801T>A (n.801T>A) | |
| 16 | g.67940165G>A | CA496383936 | LCAT | c.1062C>T (p.Gly354=) c.156-91C>T c.800C>T (n.800C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.67940165G>C | CA496383938 | LCAT | c.1062C>G (p.Gly354=) c.156-91C>G c.800C>G (n.800C>G) | |
| 16 | g.67940165G= | CA2229563239 | LCAT | c.1062C= (p.Gly354=) c.156-91C= c.800C= (n.800C=) | |
| 16 | g.67940165G>T | CA496383939 | LCAT | c.1062C>A (p.Gly354=) c.156-91C>A c.800C>A (n.800C>A) | |
| 16 | g.67940166C>A | CA396375769 | LCAT | c.1061G>T (p.Gly354Val) c.156-92G>T c.799G>T (n.799G>T) | |
| 16 | g.67940166C>G | CA396375767 | LCAT | c.1061G>C (p.Gly354Ala) c.156-92G>C c.799G>C (n.799G>C) | |
| 16 | g.67940166C>T | CA396375768 | LCAT | c.1061G>A (p.Gly354Asp) c.156-92G>A c.799G>A (n.799G>A) | |
| 16 | g.67940167C>A | CA396375770 | LCAT | c.1060G>T (p.Gly354Cys) c.156-93G>T c.798G>T (n.798G>T) | |
| 16 | g.67940167C= | CA2229563240 | LCAT | c.1060G= (p.Gly354=) c.156-93G= c.798G= (n.798G=) | |
| 16 | g.67940167C>G | CA396375771 | LCAT | c.1060G>C (p.Gly354Arg) c.156-93G>C c.798G>C (n.798G>C) | |
| 16 | g.67940167C>T | CA8120902 | LCAT | c.1060G>A (p.Gly354Ser) c.156-93G>A c.798G>A (n.798G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67940168G>A | CA496383943 | LCAT | c.1059C>T (p.His353=) c.156-94C>T c.797C>T (n.797C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.67940168G>C | CA396375772 | LCAT | c.1059C>G (p.His353Gln) c.156-94C>G c.797C>G (n.797C>G) | |
| 16 | g.67940168G= | CA2229563241 | LCAT | c.1059C= (p.His353=) c.156-94C= c.797C= (n.797C=) | |
| 16 | g.67940168G>T | CA396375773 | LCAT | c.1059C>A (p.His353Gln) c.156-94C>A c.797C>A (n.797C>A) |