Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.23808186_23808195delinsGTGGACAGCC | CA1158966142 | HMGCL | c.690_699delinsGGCTGTCCAC (p.Leu230=) c.260_269delinsGGCTGTCCAC c.*731_*740delinsGGCTGTCCAC (n.*731_*740delinsGGCTGTCCAC) c.477_486delinsGGCTGTCCAC (p.Leu159=) n.325_334delinsGGCTGTCCAC n.381_390delinsGGCTGTCCAC | |
1 | g.23808187T>A | CA339023499 | HMGCL | c.698A>T (p.His233Leu) c.268A>T c.*739A>T (n.*739A>T) c.485A>T (p.His162Leu) n.333A>T n.389A>T | |
1 | g.23808187T>C | CA234122 | HMGCL | c.698A>G (p.His233Arg) c.268A>G c.*739A>G (n.*739A>G) c.485A>G (p.His162Arg) n.333A>G n.389A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808187T>G | CA339023502 | HMGCL | c.698A>C (p.His233Pro) c.268A>C c.*739A>C (n.*739A>C) c.485A>C (p.His162Pro) n.333A>C n.389A>C | dbSNP |
1 | g.23808187T= | CA1148224190 | HMGCL | c.698A= (p.His233=) c.268A= c.*739A= (n.*739A=) c.485A= (p.His162=) n.333A= n.389A= | |
1 | g.23808187_23808195del | CA999575034 | HMGCL | c.690_698del (p.Ala231_His233del) c.260_268del c.*731_*739del (n.*731_*739del) c.477_485del (p.Ala160_His162del) n.325_333del n.381_389del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808188G>A | CA339023506 | HMGCL | c.697C>T (p.His233Tyr) c.267C>T c.*738C>T (n.*738C>T) c.484C>T (p.His162Tyr) n.332C>T n.388C>T | |
1 | g.23808188G>C | CA339023507 | HMGCL | c.697C>G (p.His233Asp) c.267C>G c.*738C>G (n.*738C>G) c.484C>G (p.His162Asp) n.332C>G n.388C>G | |
1 | g.23808188G>T | CA339023508 | HMGCL | c.697C>A (p.His233Asn) c.267C>A c.*738C>A (n.*738C>A) c.484C>A (p.His162Asn) n.332C>A n.388C>A | |
1 | g.23808190_23808198del | CA2573051539 | HMGCL | c.689_697del (p.Leu230_Val232del) c.259_267del c.*730_*738del (n.*730_*738del) c.476_484del (p.Leu159_Val161del) n.324_332del n.380_388del | ClinVar dbSNP gnomAD v4 |
1 | g.23808189G>A | CA416621156 | HMGCL | c.696C>T (p.Val232=) c.266C>T c.*737C>T (n.*737C>T) c.483C>T (p.Val161=) n.331C>T n.387C>T | gnomAD v4 |
1 | g.23808189G>C | CA416621162 | HMGCL | c.696C>G (p.Val232=) c.266C>G c.*737C>G (n.*737C>G) c.483C>G (p.Val161=) n.331C>G n.387C>G | |
1 | g.23808189G>T | CA416621158 | HMGCL | c.696C>A (p.Val232=) c.266C>A c.*737C>A (n.*737C>A) c.483C>A (p.Val161=) n.331C>A n.387C>A | |
1 | g.23808190A>C | CA339023511 | HMGCL | c.695T>G (p.Val232Gly) c.265T>G c.*736T>G (n.*736T>G) c.482T>G (p.Val161Gly) n.330T>G n.386T>G | gnomAD v4 |
1 | g.23808190A>G | CA339023517 | HMGCL | c.695T>C (p.Val232Ala) c.265T>C c.*736T>C (n.*736T>C) c.482T>C (p.Val161Ala) n.330T>C n.386T>C | |
1 | g.23808190A>T | CA339023519 | HMGCL | c.695T>A (p.Val232Asp) c.265T>A c.*736T>A (n.*736T>A) c.482T>A (p.Val161Asp) n.330T>A n.386T>A | |
1 | g.23808191C>A | CA339023523 | HMGCL | c.694G>T (p.Val232Phe) c.264G>T c.*735G>T (n.*735G>T) c.481G>T (p.Val161Phe) n.329G>T n.385G>T | |
1 | g.23808191C= | CA1158966143 | HMGCL | c.694G= (p.Val232=) c.264G= c.*735G= (n.*735G=) c.481G= (p.Val161=) n.329G= n.385G= | |
1 | g.23808191C>G | CA339023524 | HMGCL | c.694G>C (p.Val232Leu) c.264G>C c.*735G>C (n.*735G>C) c.481G>C (p.Val161Leu) n.329G>C n.385G>C | |
1 | g.23808191C>T | CA339023526 | HMGCL | c.694G>A (p.Val232Ile) c.264G>A c.*735G>A (n.*735G>A) c.481G>A (p.Val161Ile) n.329G>A n.385G>A | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808192A>C | CA416621186 | HMGCL | c.693T>G (p.Ala231=) c.263T>G c.*734T>G (n.*734T>G) c.480T>G (p.Ala160=) n.328T>G n.384T>G | |
1 | g.23808192A>G | CA416621190 | HMGCL | c.693T>C (p.Ala231=) c.263T>C c.*734T>C (n.*734T>C) c.480T>C (p.Ala160=) n.328T>C n.384T>C | |
1 | g.23808192A>T | CA416621193 | HMGCL | c.693T>A (p.Ala231=) c.263T>A c.*734T>A (n.*734T>A) c.480T>A (p.Ala160=) n.328T>A n.384T>A | |
1 | g.23808193G>A | CA339023547 | HMGCL | c.692C>T (p.Ala231Val) c.262C>T c.*733C>T (n.*733C>T) c.479C>T (p.Ala160Val) n.327C>T n.383C>T | gnomAD v4 |
1 | g.23808193G>C | CA339023540 | HMGCL | c.692C>G (p.Ala231Gly) c.262C>G c.*733C>G (n.*733C>G) c.479C>G (p.Ala160Gly) n.327C>G n.383C>G | |
1 | g.23808193G>T | CA339023544 | HMGCL | c.692C>A (p.Ala231Asp) c.262C>A c.*733C>A (n.*733C>A) c.479C>A (p.Ala160Asp) n.327C>A n.383C>A | |
1 | g.23808194C>A | CA339023549 | HMGCL | c.691G>T (p.Ala231Ser) c.261G>T c.*732G>T (n.*732G>T) c.478G>T (p.Ala160Ser) n.326G>T n.382G>T | |
1 | g.23808194C>G | CA339023556 | HMGCL | c.691G>C (p.Ala231Pro) c.261G>C c.*732G>C (n.*732G>C) c.478G>C (p.Ala160Pro) n.326G>C n.382G>C | |
1 | g.23808194C>T | CA339023559 | HMGCL | c.691G>A (p.Ala231Thr) c.261G>A c.*732G>A (n.*732G>A) c.478G>A (p.Ala160Thr) n.326G>A n.382G>A | |
1 | g.23808195C>A | CA416621205 | HMGCL | c.690G>T (p.Leu230=) c.260G>T c.*731G>T (n.*731G>T) c.477G>T (p.Leu159=) n.325G>T n.381G>T | |
1 | g.23808195C>G | CA416621211 | HMGCL | c.690G>C (p.Leu230=) c.260G>C c.*731G>C (n.*731G>C) c.477G>C (p.Leu159=) n.325G>C n.381G>C | |
1 | g.23808195C>T | CA416621213 | HMGCL | c.690G>A (p.Leu230=) c.260G>A c.*731G>A (n.*731G>A) c.477G>A (p.Leu159=) n.325G>A n.381G>A | |
1 | g.23808196A>C | CA339023563 | HMGCL | c.689T>G (p.Leu230Arg) c.259T>G c.*730T>G (n.*730T>G) c.476T>G (p.Leu159Arg) n.324T>G n.380T>G | |
1 | g.23808196A>G | CA339023566 | HMGCL | c.689T>C (p.Leu230Pro) c.259T>C c.*730T>C (n.*730T>C) c.476T>C (p.Leu159Pro) n.324T>C n.380T>C | |
1 | g.23808196A>T | CA339023567 | HMGCL | c.689T>A (p.Leu230Gln) c.259T>A c.*730T>A (n.*730T>A) c.476T>A (p.Leu159Gln) n.324T>A n.380T>A | |
1 | g.23808197G>A | CA416621222 | HMGCL | c.688C>T (p.Leu230=) c.258C>T c.*729C>T (n.*729C>T) c.475C>T (p.Leu159=) n.323C>T n.379C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.23808197G>C | CA339023570 | HMGCL | c.688C>G (p.Leu230Val) c.258C>G c.*729C>G (n.*729C>G) c.475C>G (p.Leu159Val) n.323C>G n.379C>G | |
1 | g.23808197G= | CA1158966144 | HMGCL | c.688C= (p.Leu230=) c.258C= c.*729C= (n.*729C=) c.475C= (p.Leu159=) n.323C= n.379C= | |
1 | g.23808197G>T | CA339023575 | HMGCL | c.688C>A (p.Leu230Met) c.258C>A c.*729C>A (n.*729C>A) c.475C>A (p.Leu159Met) n.323C>A n.379C>A | |
1 | g.23808199dup | CA913073224 | HMGCL | c.688dup (p.Leu230ProfsTer7) c.258dup c.*729dup (n.*729dup) c.475dup (p.Leu159ProfsTer7) n.323dup n.379dup | |
1 | g.23808198G>A | CA416621227 | HMGCL | c.687C>T (p.Ala229=) c.257C>T c.*728C>T (n.*728C>T) c.474C>T (p.Ala158=) n.322C>T n.378C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808198G>C | CA416621230 | HMGCL | c.687C>G (p.Ala229=) c.257C>G c.*728C>G (n.*728C>G) c.474C>G (p.Ala158=) n.322C>G n.378C>G | |
1 | g.23808198G= | CA1158966145 | HMGCL | c.687C= (p.Ala229=) c.257C= c.*728C= (n.*728C=) c.474C= (p.Ala158=) n.322C= n.378C= | |
1 | g.23808198G>T | CA416621231 | HMGCL | c.687C>A (p.Ala229=) c.257C>A c.*728C>A (n.*728C>A) c.474C>A (p.Ala158=) n.322C>A n.378C>A | ClinVar dbSNP |
1 | g.23808199G>A | CA686006 | HMGCL | c.686C>T (p.Ala229Val) c.256C>T c.*727C>T (n.*727C>T) c.473C>T (p.Ala158Val) n.321C>T n.377C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808199G>C | CA339023590 | HMGCL | c.686C>G (p.Ala229Gly) c.256C>G c.*727C>G (n.*727C>G) c.473C>G (p.Ala158Gly) n.321C>G n.377C>G | |
1 | g.23808199G= | CA1158966146 | HMGCL | c.686C= (p.Ala229=) c.256C= c.*727C= (n.*727C=) c.473C= (p.Ala158=) n.321C= n.377C= | |
1 | g.23808199G>T | CA339023594 | HMGCL | c.686C>A (p.Ala229Asp) c.256C>A c.*727C>A (n.*727C>A) c.473C>A (p.Ala158Asp) n.321C>A n.377C>A | ClinVar dbSNP |
1 | g.23808200_23808208dup | CA658820995 | HMGCL | c.678_686dup (p.Ala229_Leu230insLeuAlaAla) c.248_256dup c.*719_*727dup (n.*719_*727dup) c.465_473dup (p.Ala158_Leu159insLeuAlaAla) n.313_321dup n.369_377dup | ClinVar dbSNP |
1 | g.23808200C>A | CA339023602 | HMGCL | c.685G>T (p.Ala229Ser) c.255G>T c.*726G>T (n.*726G>T) c.472G>T (p.Ala158Ser) n.320G>T n.376G>T | |
1 | g.23808200C>G | CA339023605 | HMGCL | c.685G>C (p.Ala229Pro) c.255G>C c.*726G>C (n.*726G>C) c.472G>C (p.Ala158Pro) n.320G>C n.376G>C | |
1 | g.23808200C>T | CA339023600 | HMGCL | c.685G>A (p.Ala229Thr) c.255G>A c.*726G>A (n.*726G>A) c.472G>A (p.Ala158Thr) n.320G>A n.376G>A | ClinVar |
1 | g.23808201A>C | CA416621243 | HMGCL | c.684T>G (p.Ala228=) c.254T>G c.*725T>G (n.*725T>G) c.471T>G (p.Ala157=) n.319T>G n.375T>G | |
1 | g.23808201A>G | CA416621252 | HMGCL | c.684T>C (p.Ala228=) c.254T>C c.*725T>C (n.*725T>C) c.471T>C (p.Ala157=) n.319T>C n.375T>C | gnomAD v4 |
1 | g.23808201A>T | CA416621245 | HMGCL | c.684T>A (p.Ala228=) c.254T>A c.*725T>A (n.*725T>A) c.471T>A (p.Ala157=) n.319T>A n.375T>A | |
1 | g.23808202G>A | CA339023613 | HMGCL | c.683C>T (p.Ala228Val) c.253C>T c.*724C>T (n.*724C>T) c.470C>T (p.Ala157Val) n.318C>T n.374C>T | |
1 | g.23808202G>C | CA339023615 | HMGCL | c.683C>G (p.Ala228Gly) c.253C>G c.*724C>G (n.*724C>G) c.470C>G (p.Ala157Gly) n.318C>G n.374C>G | |
1 | g.23808202G>T | CA339023624 | HMGCL | c.683C>A (p.Ala228Asp) c.253C>A c.*724C>A (n.*724C>A) c.470C>A (p.Ala157Asp) n.318C>A n.374C>A | |
1 | g.23808203C>A | CA339023628 | HMGCL | c.682G>T (p.Ala228Ser) c.252G>T c.*723G>T (n.*723G>T) c.469G>T (p.Ala157Ser) n.317G>T n.373G>T | |
1 | g.23808203C>G | CA339023630 | HMGCL | c.682G>C (p.Ala228Pro) c.252G>C c.*723G>C (n.*723G>C) c.469G>C (p.Ala157Pro) n.317G>C n.373G>C | |
1 | g.23808203C>T | CA339023633 | HMGCL | c.682G>A (p.Ala228Thr) c.252G>A c.*723G>A (n.*723G>A) c.469G>A (p.Ala157Thr) n.317G>A n.373G>A | gnomAD v4 |
1 | g.23808204C>A | CA416621271 | HMGCL | c.681G>T (p.Leu227=) c.251G>T c.*722G>T (n.*722G>T) c.468G>T (p.Leu156=) n.316G>T n.372G>T | |
1 | g.23808204C>G | CA416621266 | HMGCL | c.681G>C (p.Leu227=) c.251G>C c.*722G>C (n.*722G>C) c.468G>C (p.Leu156=) n.316G>C n.372G>C | |
1 | g.23808204C>T | CA416621269 | HMGCL | c.681G>A (p.Leu227=) c.251G>A c.*722G>A (n.*722G>A) c.468G>A (p.Leu156=) n.316G>A n.372G>A | |
1 | g.23808205A>C | CA339023643 | HMGCL | c.680T>G (p.Leu227Arg) c.250T>G c.*721T>G (n.*721T>G) c.467T>G (p.Leu156Arg) n.315T>G n.371T>G | |
1 | g.23808205A>G | CA339023635 | HMGCL | c.680T>C (p.Leu227Pro) c.250T>C c.*721T>C (n.*721T>C) c.467T>C (p.Leu156Pro) n.315T>C n.371T>C | |
1 | g.23808205A>T | CA339023638 | HMGCL | c.680T>A (p.Leu227Gln) c.250T>A c.*721T>A (n.*721T>A) c.467T>A (p.Leu156Gln) n.315T>A n.371T>A | |
1 | g.23808206_23808207insCGCGATCTTCGGGCCGATGCCAGAGACCGACATGAGCGTGGTGAACACGTCGCGCTCGTCGCAGGACTCGAAGCCGTAG | CA2740117953 | HMGCL | c.680_681insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT (p.Ala228ArgfsTer35) c.250_251insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT c.*721_*722insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT (n.*721_*722insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT) c.467_468insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT (p.Ala157ArgfsTer35) n.315_316insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT n.371_372insACGGCTTCGAGTCCTGCGACGAGCGCGACGTGTTCACCACGCTCATGTCGGTCTCTGGCATCGGCCCGAAGATCGCGCT | |
1 | g.23808206G>A | CA416621277 | HMGCL | c.679C>T (p.Leu227=) c.249C>T c.*720C>T (n.*720C>T) c.466C>T (p.Leu156=) n.314C>T n.370C>T | |
1 | g.23808206G>C | CA339023648 | HMGCL | c.679C>G (p.Leu227Val) c.249C>G c.*720C>G (n.*720C>G) c.466C>G (p.Leu156Val) n.314C>G n.370C>G | |
1 | g.23808206G>T | CA339023652 | HMGCL | c.679C>A (p.Leu227Met) c.249C>A c.*720C>A (n.*720C>A) c.466C>A (p.Leu156Met) n.314C>A n.370C>A | |
1 | g.23808207A= | CA1158966147 | HMGCL | c.678T= (p.Pro226=) c.248T= c.*719T= (n.*719T=) c.465T= (p.Pro155=) n.313T= n.369T= | |
1 | g.23808207A>C | CA416621282 | HMGCL | c.678T>G (p.Pro226=) c.248T>G c.*719T>G (n.*719T>G) c.465T>G (p.Pro155=) n.313T>G n.369T>G | dbSNP gnomAD v2 |
1 | g.23808207A>G | CA416621284 | HMGCL | c.678T>C (p.Pro226=) c.248T>C c.*719T>C (n.*719T>C) c.465T>C (p.Pro155=) n.313T>C n.369T>C | |
1 | g.23808207A>T | CA416621286 | HMGCL | c.678T>A (p.Pro226=) c.248T>A c.*719T>A (n.*719T>A) c.465T>A (p.Pro155=) n.313T>A n.369T>A | |
1 | g.23808208G>A | CA339023659 | HMGCL | c.677C>T (p.Pro226Leu) c.247C>T c.*718C>T (n.*718C>T) c.464C>T (p.Pro155Leu) n.312C>T n.368C>T | gnomAD v4 |
1 | g.23808208G>C | CA339023667 | HMGCL | c.677C>G (p.Pro226Arg) c.247C>G c.*718C>G (n.*718C>G) c.464C>G (p.Pro155Arg) n.312C>G n.368C>G | |
1 | g.23808208G>T | CA339023669 | HMGCL | c.677C>A (p.Pro226His) c.247C>A c.*718C>A (n.*718C>A) c.464C>A (p.Pro155His) n.312C>A n.368C>A | |
1 | g.23808208_23808210del | CA2742818718 | HMGCL | c.675_677del (p.Pro226del) c.245_247del c.*716_*718del (n.*716_*718del) c.462_464del (p.Pro155del) n.310_312del n.366_368del | |
1 | g.23808209G>A | CA339023692 | HMGCL | c.676C>T (p.Pro226Ser) c.246C>T c.*717C>T (n.*717C>T) c.463C>T (p.Pro155Ser) n.311C>T n.367C>T | |
1 | g.23808209G>C | CA339023711 | HMGCL | c.676C>G (p.Pro226Ala) c.246C>G c.*717C>G (n.*717C>G) c.463C>G (p.Pro155Ala) n.311C>G n.367C>G | |
1 | g.23808209G>T | CA339023696 | HMGCL | c.676C>A (p.Pro226Thr) c.246C>A c.*717C>A (n.*717C>A) c.463C>A (p.Pro155Thr) n.311C>A n.367C>A | |
1 | g.23808210C>A | CA416621294 | HMGCL | c.675G>T (p.Val225=) c.245G>T c.*716G>T (n.*716G>T) c.462G>T (p.Val154=) n.310G>T n.366G>T | |
1 | g.23808210C= | CA1158966148 | HMGCL | c.675G= (p.Val225=) c.245G= c.*716G= (n.*716G=) c.462G= (p.Val154=) n.310G= n.366G= | |
1 | g.23808210C>G | CA416621297 | HMGCL | c.675G>C (p.Val225=) c.245G>C c.*716G>C (n.*716G>C) c.462G>C (p.Val154=) n.310G>C n.366G>C | ClinVar |
1 | g.23808210C>T | CA416621302 | HMGCL | c.675G>A (p.Val225=) c.245G>A c.*716G>A (n.*716G>A) c.462G>A (p.Val154=) n.310G>A n.366G>A | ClinVar dbSNP gnomAD v4 |
1 | g.23808211A= | CA1158966149 | HMGCL | c.674T= (p.Val225=) c.244T= c.*715T= (n.*715T=) c.461T= (p.Val154=) n.309T= n.365T= | |
1 | g.23808211A>C | CA339023718 | HMGCL | c.674T>G (p.Val225Gly) c.244T>G c.*715T>G (n.*715T>G) c.461T>G (p.Val154Gly) n.309T>G n.365T>G | |
1 | g.23808211A>G | CA339023724 | HMGCL | c.674T>C (p.Val225Ala) c.244T>C c.*715T>C (n.*715T>C) c.461T>C (p.Val154Ala) n.309T>C n.365T>C | dbSNP |
1 | g.23808211A>T | CA339023728 | HMGCL | c.674T>A (p.Val225Glu) c.244T>A c.*715T>A (n.*715T>A) c.461T>A (p.Val154Glu) n.309T>A n.365T>A | gnomAD v4 |
1 | g.23808212C>A | CA339023746 | HMGCL | c.673G>T (p.Val225Leu) c.243G>T c.*714G>T (n.*714G>T) c.460G>T (p.Val154Leu) n.308G>T n.364G>T | |
1 | g.23808212C>G | CA339023757 | HMGCL | c.673G>C (p.Val225Leu) c.243G>C c.*714G>C (n.*714G>C) c.460G>C (p.Val154Leu) n.308G>C n.364G>C | |
1 | g.23808212C>T | CA339023764 | HMGCL | c.673G>A (p.Val225Met) c.243G>A c.*714G>A (n.*714G>A) c.460G>A (p.Val154Met) n.308G>A n.364G>A | |
1 | g.23808213T>A | CA339023769 | HMGCL | c.672A>T (p.Glu224Asp) c.242A>T c.*713A>T (n.*713A>T) c.459A>T (p.Glu153Asp) n.307A>T n.363A>T | |
1 | g.23808213T>C | CA416621315 | HMGCL | c.672A>G (p.Glu224=) c.242A>G c.*713A>G (n.*713A>G) c.459A>G (p.Glu153=) n.307A>G n.363A>G | |
1 | g.23808213T>G | CA339023771 | HMGCL | c.672A>C (p.Glu224Asp) c.242A>C c.*713A>C (n.*713A>C) c.459A>C (p.Glu153Asp) n.307A>C n.363A>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808213_23808214insAAAATA | CA2742818719 | HMGCL | c.671_672insTATTTT (p.Glu224delinsAspIleLeu) c.241_242insTATTTT c.*712_*713insTATTTT (n.*712_*713insTATTTT) c.458_459insTATTTT (p.Glu153delinsAspIleLeu) n.306_307insTATTTT n.362_363insTATTTT | |
1 | g.23808214T>A | CA339023779 | HMGCL | c.671A>T (p.Glu224Val) c.241A>T c.*712A>T (n.*712A>T) c.458A>T (p.Glu153Val) n.306A>T n.362A>T | |
1 | g.23808214T>C | CA686007 | HMGCL | c.671A>G (p.Glu224Gly) c.241A>G c.*712A>G (n.*712A>G) c.458A>G (p.Glu153Gly) n.306A>G n.362A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808214T>G | CA339023786 | HMGCL | c.671A>C (p.Glu224Ala) c.241A>C c.*712A>C (n.*712A>C) c.458A>C (p.Glu153Ala) n.306A>C n.362A>C | |
1 | g.23808214T= | CA1158966150 | HMGCL | c.671A= (p.Glu224=) c.241A= c.*712A= (n.*712A=) c.458A= (p.Glu153=) n.306A= n.362A= | |
1 | g.23808215C>A | CA339023792 | HMGCL | c.670G>T (p.Glu224Ter) c.240G>T c.*711G>T (n.*711G>T) c.457G>T (p.Glu153Ter) n.305G>T n.361G>T | |
1 | g.23808215C>G | CA339023794 | HMGCL | c.670G>C (p.Glu224Gln) c.240G>C c.*711G>C (n.*711G>C) c.457G>C (p.Glu153Gln) n.305G>C n.361G>C | |
1 | g.23808215C>T | CA339023793 | HMGCL | c.670G>A (p.Glu224Lys) c.240G>A c.*711G>A (n.*711G>A) c.457G>A (p.Glu153Lys) n.305G>A n.361G>A | |
1 | g.23808216C>A | CA339023798 | HMGCL | c.669G>T (p.Gln223His) c.239G>T c.*710G>T (n.*710G>T) c.456G>T (p.Gln152His) n.304G>T n.361-1G>T | |
1 | g.23808216C= | CA1158966151 | HMGCL | c.669G= (p.Gln223=) c.239G= c.*710G= (n.*710G=) c.456G= (p.Gln152=) n.304G= n.361-1G= | |
1 | g.23808216C>G | CA339023803 | HMGCL | c.669G>C (p.Gln223His) c.239G>C c.*710G>C (n.*710G>C) c.456G>C (p.Gln152His) n.304G>C n.361-1G>C | |
1 | g.23808216C>T | CA416621330 | HMGCL | c.669G>A (p.Gln223=) c.239G>A c.*710G>A (n.*710G>A) c.456G>A (p.Gln152=) n.304G>A n.361-1G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.23808216_23808217insACATAT | CA2742818720 | HMGCL | c.668_669insATATGT (p.Gln223_Glu224insTyrVal) c.238_239insATATGT c.*709_*710insATATGT (n.*709_*710insATATGT) c.455_456insATATGT (p.Gln152_Glu153insTyrVal) n.303_304insATATGT n.361-2_361-1insATATGT | |
1 | g.23808217T>A | CA339023810 | HMGCL | c.668A>T (p.Gln223Leu) c.238A>T c.*709A>T (n.*709A>T) c.455A>T (p.Gln152Leu) n.303A>T n.361-2A>T | |
1 | g.23808217T>C | CA339023821 | HMGCL | c.668A>G (p.Gln223Arg) c.238A>G c.*709A>G (n.*709A>G) c.455A>G (p.Gln152Arg) n.303A>G n.361-2A>G | gnomAD v4 |
1 | g.23808217T>G | CA339023813 | HMGCL | c.668A>C (p.Gln223Pro) c.238A>C c.*709A>C (n.*709A>C) c.455A>C (p.Gln152Pro) n.303A>C n.361-2A>C | |
1 | g.23808218G>A | CA339023825 | HMGCL | c.667C>T (p.Gln223Ter) c.237C>T c.*708C>T (n.*708C>T) c.454C>T (p.Gln152Ter) n.302C>T n.361-3C>T | gnomAD v4 |
1 | g.23808218G>C | CA339023828 | HMGCL | c.667C>G (p.Gln223Glu) c.237C>G c.*708C>G (n.*708C>G) c.454C>G (p.Gln152Glu) n.302C>G n.361-3C>G | |
1 | g.23808218G>T | CA339023831 | HMGCL | c.667C>A (p.Gln223Lys) c.237C>A c.*708C>A (n.*708C>A) c.454C>A (p.Gln152Lys) n.302C>A n.361-3C>A | |
1 | g.23808219C>A | CA339023836 | HMGCL | c.666G>T (p.Met222Ile) c.236G>T c.*707G>T (n.*707G>T) c.453G>T (p.Met151Ile) n.301G>T n.361-4G>T | |
1 | g.23808219C>G | CA339023838 | HMGCL | c.666G>C (p.Met222Ile) c.236G>C c.*707G>C (n.*707G>C) c.453G>C (p.Met151Ile) n.301G>C n.361-4G>C | |
1 | g.23808219C>T | CA339023840 | HMGCL | c.666G>A (p.Met222Ile) c.236G>A c.*707G>A (n.*707G>A) c.453G>A (p.Met151Ile) n.301G>A n.361-4G>A | |
1 | g.23808220A>C | CA339023846 | HMGCL | c.665T>G (p.Met222Arg) c.235T>G c.*706T>G (n.*706T>G) c.452T>G (p.Met151Arg) n.300T>G n.361-5T>G | |
1 | g.23808220A>G | CA339023852 | HMGCL | c.665T>C (p.Met222Thr) c.235T>C c.*706T>C (n.*706T>C) c.452T>C (p.Met151Thr) n.300T>C n.361-5T>C | gnomAD v4 |
1 | g.23808220A>T | CA339023856 | HMGCL | c.665T>A (p.Met222Lys) c.235T>A c.*706T>A (n.*706T>A) c.452T>A (p.Met151Lys) n.300T>A n.361-5T>A | |
1 | g.23808221T>A | CA339023866 | HMGCL | c.664A>T (p.Met222Leu) c.234A>T c.*705A>T (n.*705A>T) c.451A>T (p.Met151Leu) n.299A>T n.361-6A>T | |
1 | g.23808221T>C | CA339023871 | HMGCL | c.664A>G (p.Met222Val) c.234A>G c.*705A>G (n.*705A>G) c.451A>G (p.Met151Val) n.299A>G n.361-6A>G | gnomAD v4 |
1 | g.23808221T>G | CA339023877 | HMGCL | c.664A>C (p.Met222Leu) c.234A>C c.*705A>C (n.*705A>C) c.451A>C (p.Met151Leu) n.299A>C n.361-6A>C | |
1 | g.23808222G>A | CA686008 | HMGCL | c.663C>T (p.Val221=) c.233C>T c.*704C>T (n.*704C>T) c.450C>T (p.Val150=) n.298C>T n.361-7C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808222G>C | CA416621358 | HMGCL | c.663C>G (p.Val221=) c.233C>G c.*704C>G (n.*704C>G) c.450C>G (p.Val150=) n.298C>G n.361-7C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808222G= | CA1141956809 | HMGCL | c.663C= (p.Val221=) c.233C= c.*704C= (n.*704C=) c.450C= (p.Val150=) n.298C= n.361-7C= | |
1 | g.23808222G>T | CA416621361 | HMGCL | c.663C>A (p.Val221=) c.233C>A c.*704C>A (n.*704C>A) c.450C>A (p.Val150=) n.298C>A n.361-7C>A | gnomAD v4 |
1 | g.23808222_23808223del | CA2742818721 | HMGCL | c.662_663del (p.Val221AspfsTer15) c.232_233del c.*703_*704del (n.*703_*704del) c.449_450del (p.Val150AspfsTer15) n.297_298del n.361-8_361-7del | |
1 | g.23808223A= | CA1158966153 | HMGCL | c.662T= (p.Val221=) c.232T= c.*703T= (n.*703T=) c.449T= (p.Val150=) n.297T= n.361-8T= | |
1 | g.23808223A>C | CA339023885 | HMGCL | c.662T>G (p.Val221Gly) c.232T>G c.*703T>G (n.*703T>G) c.449T>G (p.Val150Gly) n.297T>G n.361-8T>G | |
1 | g.23808223A>G | CA339023892 | HMGCL | c.662T>C (p.Val221Ala) c.232T>C c.*703T>C (n.*703T>C) c.449T>C (p.Val150Ala) n.297T>C n.361-8T>C | dbSNP |
1 | g.23808223A>T | CA339023897 | HMGCL | c.662T>A (p.Val221Asp) c.232T>A c.*703T>A (n.*703T>A) c.449T>A (p.Val150Asp) n.297T>A n.361-8T>A | |
1 | g.23808223_23808226delinsACAG | CA1158966152 | HMGCL | c.659_662delinsCTGT (p.Ala220=) c.229_232delinsCTGT c.*700_*703delinsCTGT (n.*700_*703delinsCTGT) c.446_449delinsCTGT (p.Ala149=) n.294_297delinsCTGT n.361-11_361-8delinsCTGT | |
1 | g.23808224C>A | CA339023899 | HMGCL | c.661G>T (p.Val221Phe) c.231G>T c.*702G>T (n.*702G>T) c.448G>T (p.Val150Phe) n.296G>T n.361-9G>T | |
1 | g.23808224C= | CA1148249053 | HMGCL | c.661G= (p.Val221=) c.231G= c.*702G= (n.*702G=) c.448G= (p.Val150=) n.296G= n.361-9G= | |
1 | g.23808224C>G | CA339023903 | HMGCL | c.661G>C (p.Val221Leu) c.231G>C c.*702G>C (n.*702G>C) c.448G>C (p.Val150Leu) n.296G>C n.361-9G>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808224C>T | CA686009 | HMGCL | c.661G>A (p.Val221Ile) c.231G>A c.*702G>A (n.*702G>A) c.448G>A (p.Val150Ile) n.296G>A n.361-9G>A | ClinVar dbSNP ExAC gnomAD v4 |
1 | g.23808227_23808229del | CA733293464 | HMGCL | c.659_661del (p.Ala220del) c.229_231del c.*700_*702del (n.*700_*702del) c.446_448del (p.Ala149del) n.294_296del n.361-11_361-9del | dbSNP |
1 | g.23808225A>C | CA416621372 | HMGCL | c.660T>G (p.Ala220=) c.230T>G c.*701T>G (n.*701T>G) c.447T>G (p.Ala149=) n.295T>G n.361-10T>G | |
1 | g.23808225A>G | CA416621378 | HMGCL | c.660T>C (p.Ala220=) c.230T>C c.*701T>C (n.*701T>C) c.447T>C (p.Ala149=) n.295T>C n.361-10T>C | |
1 | g.23808225A>T | CA416621375 | HMGCL | c.660T>A (p.Ala220=) c.230T>A c.*701T>A (n.*701T>A) c.447T>A (p.Ala149=) n.295T>A n.361-10T>A | |
1 | g.23808229_23808235del | CA2644076433 | HMGCL | c.654_660del (p.Ala220CysfsTer25) c.224_230del c.*695_*701del (n.*695_*701del) c.441_447del (p.Ala149CysfsTer25) n.289_295del n.361-16_361-10del | gnomAD v4 |
1 | g.23808226del | CA2742818722 | HMGCL | c.659del (p.Ala220ValfsTer27) c.229del c.*700del (n.*700del) c.446del (p.Ala149ValfsTer27) n.294del n.361-11del | |
1 | g.23808226G>A | CA339023912 | HMGCL | c.659C>T (p.Ala220Val) c.229C>T c.*700C>T (n.*700C>T) c.446C>T (p.Ala149Val) n.294C>T n.361-11C>T | gnomAD v4 |
1 | g.23808226G>C | CA339023919 | HMGCL | c.659C>G (p.Ala220Gly) c.229C>G c.*700C>G (n.*700C>G) c.446C>G (p.Ala149Gly) n.294C>G n.361-11C>G | |
1 | g.23808226G>T | CA339023935 | HMGCL | c.659C>A (p.Ala220Asp) c.229C>A c.*700C>A (n.*700C>A) c.446C>A (p.Ala149Asp) n.294C>A n.361-11C>A | |
1 | g.23808227del | CA658820586 | HMGCL | c.658del (p.Ala220LeufsTer27) c.228del c.*699del (n.*699del) c.445del (p.Ala149LeufsTer27) n.293del n.361-12del | gnomAD v4 |
1 | g.23808227C>A | CA339023943 | HMGCL | c.658G>T (p.Ala220Ser) c.228G>T c.*699G>T (n.*699G>T) c.445G>T (p.Ala149Ser) n.293G>T n.361-12G>T | dbSNP |
1 | g.23808227C= | CA1158966154 | HMGCL | c.658G= (p.Ala220=) c.228G= c.*699G= (n.*699G=) c.445G= (p.Ala149=) n.293G= n.361-12G= | |
1 | g.23808227C>G | CA339023949 | HMGCL | c.658G>C (p.Ala220Pro) c.228G>C c.*699G>C (n.*699G>C) c.445G>C (p.Ala149Pro) n.293G>C n.361-12G>C | gnomAD v4 |
1 | g.23808227C>T | CA339023952 | HMGCL | c.658G>A (p.Ala220Thr) c.228G>A c.*699G>A (n.*699G>A) c.445G>A (p.Ala149Thr) n.293G>A n.361-12G>A | |
1 | g.23808227_23808228insTT | CA2742818723 | HMGCL | c.657_658insAA (p.Ala220LysfsTer28) c.227_228insAA c.*698_*699insAA (n.*698_*699insAA) c.444_445insAA (p.Ala149LysfsTer28) n.292_293insAA n.361-13_361-12insAA | |
1 | g.23808228A>C | CA416621395 | HMGCL | c.657T>G (p.Ser219=) c.227T>G c.*698T>G (n.*698T>G) c.444T>G (p.Ser148=) n.292T>G n.361-13T>G | |
1 | g.23808228A>G | CA416621389 | HMGCL | c.657T>C (p.Ser219=) c.227T>C c.*698T>C (n.*698T>C) c.444T>C (p.Ser148=) n.292T>C n.361-13T>C | |
1 | g.23808228A>T | CA416621392 | HMGCL | c.657T>A (p.Ser219=) c.227T>A c.*698T>A (n.*698T>A) c.444T>A (p.Ser148=) n.292T>A n.361-13T>A | |
1 | g.23808229G>A | CA339023964 | HMGCL | c.656C>T (p.Ser219Phe) c.226C>T c.*697C>T (n.*697C>T) c.443C>T (p.Ser148Phe) n.291C>T n.361-14C>T | |
1 | g.23808229G>C | CA339023960 | HMGCL | c.656C>G (p.Ser219Cys) c.226C>G c.*697C>G (n.*697C>G) c.443C>G (p.Ser148Cys) n.291C>G n.361-14C>G | |
1 | g.23808229G>T | CA339023957 | HMGCL | c.656C>A (p.Ser219Tyr) c.226C>A c.*697C>A (n.*697C>A) c.443C>A (p.Ser148Tyr) n.291C>A n.361-14C>A | COSMIC |
1 | g.23808230A>C | CA339023969 | HMGCL | c.655T>G (p.Ser219Ala) c.225T>G c.*696T>G (n.*696T>G) c.442T>G (p.Ser148Ala) n.290T>G n.361-15T>G | |
1 | g.23808230A>G | CA339023967 | HMGCL | c.655T>C (p.Ser219Pro) c.225T>C c.*696T>C (n.*696T>C) c.442T>C (p.Ser148Pro) n.290T>C n.361-15T>C | |
1 | g.23808230A>T | CA339023968 | HMGCL | c.655T>A (p.Ser219Thr) c.225T>A c.*696T>A (n.*696T>A) c.442T>A (p.Ser148Thr) n.290T>A n.361-15T>A | |
1 | g.23808231T>A | CA416621405 | HMGCL | c.654A>T (p.Leu218=) c.224A>T c.*695A>T (n.*695A>T) c.441A>T (p.Leu147=) n.289A>T n.361-16A>T | gnomAD v3 gnomAD v4 |
1 | g.23808231T>C | CA285335 | HMGCL | c.654A>G (p.Leu218=) c.224A>G c.*695A>G (n.*695A>G) c.441A>G (p.Leu147=) n.289A>G n.361-16A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808231T>G | CA416621409 | HMGCL | c.654A>C (p.Leu218=) c.224A>C c.*695A>C (n.*695A>C) c.441A>C (p.Leu147=) n.289A>C n.361-16A>C | |
1 | g.23808231T= | CA1139826944 | HMGCL | c.654A= (p.Leu218=) c.224A= c.*695A= (n.*695A=) c.441A= (p.Leu147=) n.289A= n.361-16A= | |
1 | g.23808231_23808232insGC | CA999575070 | HMGCL | c.653_654insGC (p.Ser219HisfsTer29) c.223_224insGC c.*694_*695insGC (n.*694_*695insGC) c.440_441insGC (p.Ser148HisfsTer29) n.288_289insGC n.361-17_361-16insGC | gnomAD v3 gnomAD v4 |
1 | g.23808231_23808232insTCCTGCATGACAGCAGAC | CA999575075 | HMGCL | c.653_654insGTCTGCTGTCATGCAGGA (p.Leu218_Ser219insSerAlaValMetGlnGlu) c.223_224insGTCTGCTGTCATGCAGGA c.*694_*695insGTCTGCTGTCATGCAGGA (n.*694_*695insGTCTGCTGTCATGCAGGA) c.440_441insGTCTGCTGTCATGCAGGA (p.Leu147_Ser148insSerAlaValMetGlnGlu) n.288_289insGTCTGCTGTCATGCAGGA n.361-17_361-16insGTCTGCTGTCATGCAGGA | gnomAD v3 gnomAD v4 |
1 | g.23808232A= | CA1158966155 | HMGCL | c.653T= (p.Leu218=) c.223T= c.*694T= (n.*694T=) c.440T= (p.Leu147=) n.288T= n.361-17T= | |
1 | g.23808232A>C | CA339023972 | HMGCL | c.653T>G (p.Leu218Arg) c.223T>G c.*694T>G (n.*694T>G) c.440T>G (p.Leu147Arg) n.288T>G n.361-17T>G | |
1 | g.23808232A>G | CA339023973 | HMGCL | c.653T>C (p.Leu218Pro) c.223T>C c.*694T>C (n.*694T>C) c.440T>C (p.Leu147Pro) n.288T>C n.361-17T>C | dbSNP gnomAD v2 |
1 | g.23808232A>T | CA339023974 | HMGCL | c.653T>A (p.Leu218Gln) c.223T>A c.*694T>A (n.*694T>A) c.440T>A (p.Leu147Gln) n.288T>A n.361-17T>A | |
1 | g.23808233G>A | CA686010 | HMGCL | c.652C>T (p.Leu218=) c.222C>T c.*693C>T (n.*693C>T) c.439C>T (p.Leu147=) n.287C>T n.361-18C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808233G>C | CA339023979 | HMGCL | c.652C>G (p.Leu218Val) c.222C>G c.*693C>G (n.*693C>G) c.439C>G (p.Leu147Val) n.287C>G n.361-18C>G | |
1 | g.23808233G= | CA1158966156 | HMGCL | c.652C= (p.Leu218=) c.222C= c.*693C= (n.*693C=) c.439C= (p.Leu147=) n.287C= n.361-18C= | |
1 | g.23808233G>T | CA339023983 | HMGCL | c.652C>A (p.Leu218Ile) c.222C>A c.*693C>A (n.*693C>A) c.439C>A (p.Leu147Ile) n.287C>A n.361-18C>A | |
1 | g.23808234C>A | CA686011 | HMGCL | c.651G>T (p.Met217Ile) c.221G>T c.*692G>T (n.*692G>T) c.438G>T (p.Met146Ile) n.286G>T n.361-19G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.23808234C= | CA1148425855 | HMGCL | c.651G= (p.Met217=) c.221G= c.*692G= (n.*692G=) c.438G= (p.Met146=) n.286G= n.361-19G= | |
1 | g.23808234C>G | CA339023988 | HMGCL | c.651G>C (p.Met217Ile) c.221G>C c.*692G>C (n.*692G>C) c.438G>C (p.Met146Ile) n.286G>C n.361-19G>C | |
1 | g.23808234C>T | CA339023990 | HMGCL | c.651G>A (p.Met217Ile) c.221G>A c.*692G>A (n.*692G>A) c.438G>A (p.Met146Ile) n.286G>A n.361-19G>A | |
1 | g.23808235A>C | CA339024013 | HMGCL | c.650T>G (p.Met217Arg) c.220T>G c.*691T>G (n.*691T>G) c.437T>G (p.Met146Arg) n.285T>G n.361-20T>G | |
1 | g.23808235A>G | CA339024002 | HMGCL | c.650T>C (p.Met217Thr) c.220T>C c.*691T>C (n.*691T>C) c.437T>C (p.Met146Thr) n.285T>C n.361-20T>C | |
1 | g.23808235A>T | CA339023995 | HMGCL | c.650T>A (p.Met217Lys) c.220T>A c.*691T>A (n.*691T>A) c.437T>A (p.Met146Lys) n.285T>A n.361-20T>A | |
1 | g.23808235_23808236insC | CA2742818725 | HMGCL | c.649_650insG (p.Met217SerfsTer20) c.219_220insG c.*690_*691insG (n.*690_*691insG) c.436_437insG (p.Met146SerfsTer20) n.284_285insG n.361-21_361-20insG | |
1 | g.23808236T>A | CA339024016 | HMGCL | c.649A>T (p.Met217Leu) c.219A>T c.*690A>T (n.*690A>T) c.436A>T (p.Met146Leu) n.284A>T n.361-21A>T | |
1 | g.23808236T>C | CA686012 | HMGCL | c.649A>G (p.Met217Val) c.219A>G c.*690A>G (n.*690A>G) c.436A>G (p.Met146Val) n.284A>G n.361-21A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808236T>G | CA339024017 | HMGCL | c.649A>C (p.Met217Leu) c.219A>C c.*690A>C (n.*690A>C) c.436A>C (p.Met146Leu) n.284A>C n.361-21A>C | |
1 | g.23808236T= | CA1158966157 | HMGCL | c.649A= (p.Met217=) c.219A= c.*690A= (n.*690A=) c.436A= (p.Met146=) n.284A= n.361-21A= | |
1 | g.23808237G>A | CA416621434 | HMGCL | c.648C>T (p.Asp216=) c.218C>T c.*689C>T (n.*689C>T) c.435C>T (p.Asp145=) n.283C>T n.361-22C>T | |
1 | g.23808237G>C | CA339024020 | HMGCL | c.648C>G (p.Asp216Glu) c.218C>G c.*689C>G (n.*689C>G) c.435C>G (p.Asp145Glu) n.283C>G n.361-22C>G | |
1 | g.23808237G>T | CA339024021 | HMGCL | c.648C>A (p.Asp216Glu) c.218C>A c.*689C>A (n.*689C>A) c.435C>A (p.Asp145Glu) n.283C>A n.361-22C>A | |
1 | g.23808238T>A | CA339024029 | HMGCL | c.647A>T (p.Asp216Val) c.217A>T c.*688A>T (n.*688A>T) c.434A>T (p.Asp145Val) n.282A>T n.361-23A>T | |
1 | g.23808238T>C | CA339024041 | HMGCL | c.647A>G (p.Asp216Gly) c.217A>G c.*688A>G (n.*688A>G) c.434A>G (p.Asp145Gly) n.282A>G n.361-23A>G | |
1 | g.23808238T>G | CA339024043 | HMGCL | c.647A>C (p.Asp216Ala) c.217A>C c.*688A>C (n.*688A>C) c.434A>C (p.Asp145Ala) n.282A>C n.361-23A>C | |
1 | g.23808239del | CA2742818726 | HMGCL | c.646del (p.Asp216ThrfsTer?) c.216del c.*687del (n.*687del) c.433del (p.Asp145ThrfsTer?) n.281del n.361-24del | |
1 | g.23808239C>A | CA339024046 | HMGCL | c.646G>T (p.Asp216Tyr) c.216G>T c.*687G>T (n.*687G>T) c.433G>T (p.Asp145Tyr) n.281G>T n.361-24G>T | |
1 | g.23808239C>G | CA339024047 | HMGCL | c.646G>C (p.Asp216His) c.216G>C c.*687G>C (n.*687G>C) c.433G>C (p.Asp145His) n.281G>C n.361-24G>C | |
1 | g.23808239C>T | CA339024048 | HMGCL | c.646G>A (p.Asp216Asn) c.216G>A c.*687G>A (n.*687G>A) c.433G>A (p.Asp145Asn) n.281G>A n.361-24G>A | |
1 | g.23808239_23808240delinsCT | CA1158966158 | HMGCL | c.645_646delinsAG (p.Lys215=) c.215_216delinsAG c.*686_*687delinsAG (n.*686_*687delinsAG) c.432_433delinsAG (p.Lys144=) n.280_281delinsAG n.361-25_361-24delinsAG | |
1 | g.23808240T>A | CA339024052 | HMGCL | c.645A>T (p.Lys215Asn) c.215A>T c.*686A>T (n.*686A>T) c.432A>T (p.Lys144Asn) n.280A>T n.361-25A>T | |
1 | g.23808240T>C | CA416621448 | HMGCL | c.645A>G (p.Lys215=) c.215A>G c.*686A>G (n.*686A>G) c.432A>G (p.Lys144=) n.280A>G n.361-25A>G | gnomAD v3 gnomAD v4 |
1 | g.23808240T>G | CA339024059 | HMGCL | c.645A>C (p.Lys215Asn) c.215A>C c.*686A>C (n.*686A>C) c.432A>C (p.Lys144Asn) n.280A>C n.361-25A>C | |
1 | g.23808242del | CA733293495 | HMGCL | c.645del (p.Asp216ThrfsTer?) c.215del c.*686del (n.*686del) c.432del (p.Asp145ThrfsTer?) n.280del n.361-25del | dbSNP |
1 | g.23808241T>A | CA339024069 | HMGCL | c.644A>T (p.Lys215Ile) c.214A>T c.*685A>T (n.*685A>T) c.431A>T (p.Lys144Ile) n.279A>T n.361-26A>T | |
1 | g.23808241T>C | CA339024070 | HMGCL | c.644A>G (p.Lys215Arg) c.214A>G c.*685A>G (n.*685A>G) c.431A>G (p.Lys144Arg) n.279A>G n.361-26A>G | |
1 | g.23808241T>G | CA339024064 | HMGCL | c.644A>C (p.Lys215Thr) c.214A>C c.*685A>C (n.*685A>C) c.431A>C (p.Lys144Thr) n.279A>C n.361-26A>C | |
1 | g.23808242T>A | CA339024071 | HMGCL | c.643A>T (p.Lys215Ter) c.213A>T c.*684A>T (n.*684A>T) c.430A>T (p.Lys144Ter) n.278A>T n.361-27A>T | |
1 | g.23808242T>C | CA339024076 | HMGCL | c.643A>G (p.Lys215Glu) c.213A>G c.*684A>G (n.*684A>G) c.430A>G (p.Lys144Glu) n.278A>G n.361-27A>G | |
1 | g.23808242T>G | CA339024074 | HMGCL | c.643A>C (p.Lys215Gln) c.213A>C c.*684A>C (n.*684A>C) c.430A>C (p.Lys144Gln) n.278A>C n.361-27A>C | |
1 | g.23808243C>A | CA339024093 | HMGCL | c.642G>T (p.Met214Ile) c.212G>T c.*683G>T (n.*683G>T) c.429G>T (p.Met143Ile) n.277G>T n.361-28G>T | |
1 | g.23808243C= | CA1158966159 | HMGCL | c.642G= (p.Met214=) c.212G= c.*683G= (n.*683G=) c.429G= (p.Met143=) n.277G= n.361-28G= | |
1 | g.23808243C>G | CA19292124 | HMGCL | c.642G>C (p.Met214Ile) c.212G>C c.*683G>C (n.*683G>C) c.429G>C (p.Met143Ile) n.277G>C n.361-28G>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808243C>T | CA339024103 | HMGCL | c.642G>A (p.Met214Ile) c.212G>A c.*683G>A (n.*683G>A) c.429G>A (p.Met143Ile) n.277G>A n.361-28G>A | |
1 | g.23808244A= | CA1158966160 | HMGCL | c.641T= (p.Met214=) c.211T= c.*682T= (n.*682T=) c.428T= (p.Met143=) n.276T= n.361-29T= | |
1 | g.23808244A>C | CA339024104 | HMGCL | c.641T>G (p.Met214Arg) c.211T>G c.*682T>G (n.*682T>G) c.428T>G (p.Met143Arg) n.276T>G n.361-29T>G | |
1 | g.23808244A>G | CA339024107 | HMGCL | c.641T>C (p.Met214Thr) c.211T>C c.*682T>C (n.*682T>C) c.428T>C (p.Met143Thr) n.276T>C n.361-29T>C | dbSNP gnomAD v4 |
1 | g.23808244A>T | CA339024108 | HMGCL | c.641T>A (p.Met214Lys) c.211T>A c.*682T>A (n.*682T>A) c.428T>A (p.Met143Lys) n.276T>A n.361-29T>A | |
1 | g.23808244_23808245insCCCTGC | CA2742818731 | HMGCL | c.640_641insGCAGGG (p.Met214delinsSerArgVal) c.210_211insGCAGGG c.*681_*682insGCAGGG (n.*681_*682insGCAGGG) c.427_428insGCAGGG (p.Met143delinsSerArgVal) n.275_276insGCAGGG n.361-30_361-29insGCAGGG | |
1 | g.23808245T>A | CA339024109 | HMGCL | c.640A>T (p.Met214Leu) c.210A>T c.*681A>T (n.*681A>T) c.427A>T (p.Met143Leu) n.275A>T n.361-30A>T | |
1 | g.23808245T>C | CA339024113 | HMGCL | c.640A>G (p.Met214Val) c.210A>G c.*681A>G (n.*681A>G) c.427A>G (p.Met143Val) n.275A>G n.361-30A>G | |
1 | g.23808245T>G | CA339024116 | HMGCL | c.640A>C (p.Met214Leu) c.210A>C c.*681A>C (n.*681A>C) c.427A>C (p.Met143Leu) n.275A>C n.361-30A>C | |
1 | g.23808246G>A | CA416621476 | HMGCL | c.639C>T (p.Ile213=) c.209C>T c.*680C>T (n.*680C>T) c.426C>T (p.Ile142=) n.274C>T n.361-31C>T | |
1 | g.23808246G>C | CA339024121 | HMGCL | c.639C>G (p.Ile213Met) c.209C>G c.*680C>G (n.*680C>G) c.426C>G (p.Ile142Met) n.274C>G n.361-31C>G | |
1 | g.23808246G>T | CA416621480 | HMGCL | c.639C>A (p.Ile213=) c.209C>A c.*680C>A (n.*680C>A) c.426C>A (p.Ile142=) n.274C>A n.361-31C>A | gnomAD v4 |
1 | g.23808247A>C | CA339024124 | HMGCL | c.638T>G (p.Ile213Ser) c.208T>G c.*679T>G (n.*679T>G) c.425T>G (p.Ile142Ser) n.273T>G n.361-32T>G | |
1 | g.23808247A>G | CA339024132 | HMGCL | c.638T>C (p.Ile213Thr) c.208T>C c.*679T>C (n.*679T>C) c.425T>C (p.Ile142Thr) n.273T>C n.361-32T>C | |
1 | g.23808247A>T | CA339024137 | HMGCL | c.638T>A (p.Ile213Asn) c.208T>A c.*679T>A (n.*679T>A) c.425T>A (p.Ile142Asn) n.273T>A n.361-32T>A | |
1 | g.23808247_23808248insGCC | CA2742818733 | HMGCL | c.637_638insGGC (p.Ile213delinsArgLeu) c.207_208insGGC c.*678_*679insGGC (n.*678_*679insGGC) c.424_425insGGC (p.Ile142delinsArgLeu) n.272_273insGGC n.361-33_361-32insGGC | |
1 | g.23808248T>A | CA339024140 | HMGCL | c.637A>T (p.Ile213Phe) c.207A>T c.*678A>T (n.*678A>T) c.424A>T (p.Ile142Phe) n.272A>T n.361-33A>T | |
1 | g.23808248T>C | CA686013 | HMGCL | c.637A>G (p.Ile213Val) c.207A>G c.*678A>G (n.*678A>G) c.424A>G (p.Ile142Val) n.272A>G n.361-33A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808248T>G | CA339024143 | HMGCL | c.637A>C (p.Ile213Leu) c.207A>C c.*678A>C (n.*678A>C) c.424A>C (p.Ile142Leu) n.272A>C n.361-33A>C | |
1 | g.23808248T= | CA1158966161 | HMGCL | c.637A= (p.Ile213=) c.207A= c.*678A= (n.*678A=) c.424A= (p.Ile142=) n.272A= n.361-33A= | |
1 | g.23808249C>A | CA416621491 | HMGCL | c.636G>T (p.Gly212=) c.206G>T c.*677G>T (n.*677G>T) c.423G>T (p.Gly141=) n.271G>T n.361-34G>T | |
1 | g.23808249C= | CA1158966162 | HMGCL | c.636G= (p.Gly212=) c.206G= c.*677G= (n.*677G=) c.423G= (p.Gly141=) n.271G= n.361-34G= | |
1 | g.23808249C>G | CA416621495 | HMGCL | c.636G>C (p.Gly212=) c.206G>C c.*677G>C (n.*677G>C) c.423G>C (p.Gly141=) n.271G>C n.361-34G>C | |
1 | g.23808249C>T | CA416621493 | HMGCL | c.636G>A (p.Gly212=) c.206G>A c.*677G>A (n.*677G>A) c.423G>A (p.Gly141=) n.271G>A n.361-34G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808250C>A | CA339024151 | HMGCL | c.635G>T (p.Gly212Val) c.205G>T c.*676G>T (n.*676G>T) c.422G>T (p.Gly141Val) n.270G>T n.361-35G>T | |
1 | g.23808250C= | CA1158966163 | HMGCL | c.635G= (p.Gly212=) c.205G= c.*676G= (n.*676G=) c.422G= (p.Gly141=) n.270G= n.361-35G= | |
1 | g.23808250C>G | CA339024153 | HMGCL | c.635G>C (p.Gly212Ala) c.205G>C c.*676G>C (n.*676G>C) c.422G>C (p.Gly141Ala) n.270G>C n.361-35G>C | |
1 | g.23808250C>T | CA339024156 | HMGCL | c.635G>A (p.Gly212Glu) c.205G>A c.*676G>A (n.*676G>A) c.422G>A (p.Gly141Glu) n.270G>A n.361-35G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.23808251C>A | CA339024158 | HMGCL | c.634G>T (p.Gly212Trp) c.204G>T c.*675G>T (n.*675G>T) c.421G>T (p.Gly141Trp) n.269G>T n.361-36G>T | |
1 | g.23808251C>G | CA339024159 | HMGCL | c.634G>C (p.Gly212Arg) c.204G>C c.*675G>C (n.*675G>C) c.421G>C (p.Gly141Arg) n.269G>C n.361-36G>C | gnomAD v4 |
1 | g.23808251C>T | CA339024165 | HMGCL | c.634G>A (p.Gly212Arg) c.204G>A c.*675G>A (n.*675G>A) c.421G>A (p.Gly141Arg) n.269G>A n.361-36G>A | |
1 | g.23808252T>A | CA416621505 | HMGCL | c.633A>T (p.Pro211=) c.203A>T c.*674A>T (n.*674A>T) c.420A>T (p.Pro140=) n.268A>T n.361-37A>T | |
1 | g.23808252T>C | CA416621503 | HMGCL | c.633A>G (p.Pro211=) c.203A>G c.*674A>G (n.*674A>G) c.420A>G (p.Pro140=) n.268A>G n.361-37A>G | gnomAD v4 |
1 | g.23808252T>G | CA416621504 | HMGCL | c.633A>C (p.Pro211=) c.203A>C c.*674A>C (n.*674A>C) c.420A>C (p.Pro140=) n.268A>C n.361-37A>C | |
1 | g.23808253G>A | CA339024169 | HMGCL | c.632C>T (p.Pro211Leu) c.202C>T c.*673C>T (n.*673C>T) c.419C>T (p.Pro140Leu) n.267C>T n.361-38C>T | |
1 | g.23808253G>C | CA339024171 | HMGCL | c.632C>G (p.Pro211Arg) c.202C>G c.*673C>G (n.*673C>G) c.419C>G (p.Pro140Arg) n.267C>G n.361-38C>G | dbSNP gnomAD v4 |
1 | g.23808253G= | CA1158966164 | HMGCL | c.632C= (p.Pro211=) c.202C= c.*673C= (n.*673C=) c.419C= (p.Pro140=) n.267C= n.361-38C= | |
1 | g.23808253G>T | CA339024172 | HMGCL | c.632C>A (p.Pro211Gln) c.202C>A c.*673C>A (n.*673C>A) c.419C>A (p.Pro140Gln) n.267C>A n.361-38C>A | |
1 | g.23808254G>A | CA339024179 | HMGCL | c.631C>T (p.Pro211Ser) c.201C>T c.*672C>T (n.*672C>T) c.418C>T (p.Pro140Ser) n.266C>T n.361-39C>T | |
1 | g.23808254G>C | CA339024178 | HMGCL | c.631C>G (p.Pro211Ala) c.201C>G c.*672C>G (n.*672C>G) c.418C>G (p.Pro140Ala) n.266C>G n.361-39C>G | |
1 | g.23808254G>T | CA339024176 | HMGCL | c.631C>A (p.Pro211Thr) c.201C>A c.*672C>A (n.*672C>A) c.418C>A (p.Pro140Thr) n.266C>A n.361-39C>A | |
1 | g.23808255G>A | CA10610714 | HMGCL | c.630C>T (p.Thr210=) c.200C>T c.*671C>T (n.*671C>T) c.417C>T (p.Thr139=) n.265C>T n.361-40C>T | ClinVar dbSNP gnomAD v4 |
1 | g.23808255G>C | CA416621525 | HMGCL | c.630C>G (p.Thr210=) c.200C>G c.*671C>G (n.*671C>G) c.417C>G (p.Thr139=) n.265C>G n.361-40C>G | |
1 | g.23808255G= | CA1158966165 | HMGCL | c.630C= (p.Thr210=) c.200C= c.*671C= (n.*671C=) c.417C= (p.Thr139=) n.265C= n.361-40C= | |
1 | g.23808255G>T | CA416621527 | HMGCL | c.630C>A (p.Thr210=) c.200C>A c.*671C>A (n.*671C>A) c.417C>A (p.Thr139=) n.265C>A n.361-40C>A | |
1 | g.23808256G>A | CA339024181 | HMGCL | c.629C>T (p.Thr210Ile) c.199C>T c.*670C>T (n.*670C>T) c.416C>T (p.Thr139Ile) n.264C>T n.361-41C>T | ClinVar dbSNP gnomAD v4 |
1 | g.23808256G>C | CA339024183 | HMGCL | c.629C>G (p.Thr210Ser) c.199C>G c.*670C>G (n.*670C>G) c.416C>G (p.Thr139Ser) n.264C>G n.361-41C>G | |
1 | g.23808256G= | CA1158966166 | HMGCL | c.629C= (p.Thr210=) c.199C= c.*670C= (n.*670C=) c.416C= (p.Thr139=) n.264C= n.361-41C= | |
1 | g.23808256G>T | CA339024186 | HMGCL | c.629C>A (p.Thr210Asn) c.199C>A c.*670C>A (n.*670C>A) c.416C>A (p.Thr139Asn) n.264C>A n.361-41C>A | |
1 | g.23808256_23808257insACA | CA2742818736 | HMGCL | c.628_629insTGT (p.Thr210delinsMetSer) c.198_199insTGT c.*669_*670insTGT (n.*669_*670insTGT) c.415_416insTGT (p.Thr139delinsMetSer) n.263_264insTGT n.361-42_361-41insTGT | |
1 | g.23808257T>A | CA339024189 | HMGCL | c.628A>T (p.Thr210Ser) c.198A>T c.*669A>T (n.*669A>T) c.415A>T (p.Thr139Ser) n.263A>T n.361-42A>T | |
1 | g.23808257T>C | CA339024191 | HMGCL | c.628A>G (p.Thr210Ala) c.198A>G c.*669A>G (n.*669A>G) c.415A>G (p.Thr139Ala) n.263A>G n.361-42A>G | |
1 | g.23808257T>G | CA339024194 | HMGCL | c.628A>C (p.Thr210Pro) c.198A>C c.*669A>C (n.*669A>C) c.415A>C (p.Thr139Pro) n.263A>C n.361-42A>C | |
1 | g.23808257_23808258insATA | CA2742818737 | HMGCL | c.627_628insTAT (p.Gly209_Thr210insTyr) c.197_198insTAT c.*668_*669insTAT (n.*668_*669insTAT) c.414_415insTAT (p.Gly138_Thr139insTyr) n.262_263insTAT n.361-43_361-42insTAT | |
1 | g.23808258G>A | CA416621540 | HMGCL | c.627C>T (p.Gly209=) c.197C>T c.*668C>T (n.*668C>T) c.414C>T (p.Gly138=) n.262C>T n.361-43C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808258G>C | CA416621542 | HMGCL | c.627C>G (p.Gly209=) c.197C>G c.*668C>G (n.*668C>G) c.414C>G (p.Gly138=) n.262C>G n.361-43C>G | |
1 | g.23808258G= | CA1158966167 | HMGCL | c.627C= (p.Gly209=) c.197C= c.*668C= (n.*668C=) c.414C= (p.Gly138=) n.262C= n.361-43C= | |
1 | g.23808258G>T | CA416621544 | HMGCL | c.627C>A (p.Gly209=) c.197C>A c.*668C>A (n.*668C>A) c.414C>A (p.Gly138=) n.262C>A n.361-43C>A | ClinVar |
1 | g.23808259C>A | CA339024196 | HMGCL | c.626G>T (p.Gly209Val) c.196G>T c.*667G>T (n.*667G>T) c.413G>T (p.Gly138Val) n.261G>T n.361-44G>T | |
1 | g.23808259C>G | CA339024198 | HMGCL | c.626G>C (p.Gly209Ala) c.196G>C c.*667G>C (n.*667G>C) c.413G>C (p.Gly138Ala) n.261G>C n.361-44G>C | |
1 | g.23808259C>T | CA339024199 | HMGCL | c.626G>A (p.Gly209Asp) c.196G>A c.*667G>A (n.*667G>A) c.413G>A (p.Gly138Asp) n.261G>A n.361-44G>A | |
1 | g.23808260C>A | CA339024200 | HMGCL | c.625G>T (p.Gly209Cys) c.195G>T c.*666G>T (n.*666G>T) c.412G>T (p.Gly138Cys) n.260G>T n.361-45G>T | |
1 | g.23808260C>G | CA339024201 | HMGCL | c.625G>C (p.Gly209Arg) c.195G>C c.*666G>C (n.*666G>C) c.412G>C (p.Gly138Arg) n.260G>C n.361-45G>C | |
1 | g.23808260C>T | CA339024203 | HMGCL | c.625G>A (p.Gly209Ser) c.195G>A c.*666G>A (n.*666G>A) c.412G>A (p.Gly138Ser) n.260G>A n.361-45G>A | |
1 | g.23808260_23808261insAAAG | CA2742818738 | HMGCL | c.624_625insCTTT (p.Gly209LeufsTer29) c.194_195insCTTT c.*665_*666insCTTT (n.*665_*666insCTTT) c.411_412insCTTT (p.Gly138LeufsTer29) n.259_260insCTTT n.361-46_361-45insCTTT | |
1 | g.23808261C>A | CA416621559 | HMGCL | c.624G>T (p.Val208=) c.194G>T c.*665G>T (n.*665G>T) c.411G>T (p.Val137=) n.259G>T n.361-46G>T | |
1 | g.23808261C= | CA1148483401 | HMGCL | c.624G= (p.Val208=) c.194G= c.*665G= (n.*665G=) c.411G= (p.Val137=) n.259G= n.361-46G= | |
1 | g.23808261C>G | CA416621560 | HMGCL | c.624G>C (p.Val208=) c.194G>C c.*665G>C (n.*665G>C) c.411G>C (p.Val137=) n.259G>C n.361-46G>C | |
1 | g.23808261C>T | CA686014 | HMGCL | c.624G>A (p.Val208=) c.194G>A c.*665G>A (n.*665G>A) c.411G>A (p.Val137=) n.259G>A n.361-46G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808262A>C | CA339024208 | HMGCL | c.623T>G (p.Val208Gly) c.193T>G c.*664T>G (n.*664T>G) c.410T>G (p.Val137Gly) n.258T>G n.361-47T>G | |
1 | g.23808262A>G | CA339024210 | HMGCL | c.623T>C (p.Val208Ala) c.193T>C c.*664T>C (n.*664T>C) c.410T>C (p.Val137Ala) n.258T>C n.361-47T>C | |
1 | g.23808262A>T | CA339024212 | HMGCL | c.623T>A (p.Val208Glu) c.193T>A c.*664T>A (n.*664T>A) c.410T>A (p.Val137Glu) n.258T>A n.361-47T>A | |
1 | g.23808262_23808263insATTTTTTTAAAATAC | CA2742818739 | HMGCL | c.622_623insGTATTTTAAAAAAAT (p.Val208delinsGlyIleLeuLysLysLeu) c.192_193insGTATTTTAAAAAAAT c.*663_*664insGTATTTTAAAAAAAT (n.*663_*664insGTATTTTAAAAAAAT) c.409_410insGTATTTTAAAAAAAT (p.Val137delinsGlyIleLeuLysLysLeu) n.257_258insGTATTTTAAAAAAAT n.361-48_361-47insGTATTTTAAAAAAAT | |
1 | g.23808263C>A | CA339024217 | HMGCL | c.622G>T (p.Val208Leu) c.192G>T c.*663G>T (n.*663G>T) c.409G>T (p.Val137Leu) n.257G>T n.361-48G>T | |
1 | g.23808263C= | CA1158966168 | HMGCL | c.622G= (p.Val208=) c.192G= c.*663G= (n.*663G=) c.409G= (p.Val137=) n.257G= n.361-48G= | |
1 | g.23808263C>G | CA686016 | HMGCL | c.622G>C (p.Val208Leu) c.192G>C c.*663G>C (n.*663G>C) c.409G>C (p.Val137Leu) n.257G>C n.361-48G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808263C>T | CA686015 | HMGCL | c.622G>A (p.Val208Met) c.192G>A c.*663G>A (n.*663G>A) c.409G>A (p.Val137Met) n.257G>A n.361-48G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808264del | CA2550505816 | HMGCL | c.621del (p.Val208TrpfsTer7) c.191del c.*662del (n.*662del) c.408del (p.Val137TrpfsTer7) n.256del n.361-49del | ClinVar dbSNP |
1 | g.23808264A= | CA1158966169 | HMGCL | c.621T= (p.Gly207=) c.191T= c.*662T= (n.*662T=) c.408T= (p.Gly136=) n.256T= n.361-49T= | |
1 | g.23808264A>C | CA416621573 | HMGCL | c.621T>G (p.Gly207=) c.191T>G c.*662T>G (n.*662T>G) c.408T>G (p.Gly136=) n.256T>G n.361-49T>G | ClinVar dbSNP |
1 | g.23808264A>G | CA416621570 | HMGCL | c.621T>C (p.Gly207=) c.191T>C c.*662T>C (n.*662T>C) c.408T>C (p.Gly136=) n.256T>C n.361-49T>C | dbSNP |
1 | g.23808264A>T | CA416621571 | HMGCL | c.621T>A (p.Gly207=) c.191T>A c.*662T>A (n.*662T>A) c.408T>A (p.Gly136=) n.256T>A n.361-49T>A | |
1 | g.23808265C>A | CA339024223 | HMGCL | c.620G>T (p.Gly207Val) c.190G>T c.*661G>T (n.*661G>T) c.407G>T (p.Gly136Val) n.255G>T n.361-50G>T | gnomAD v4 |
1 | g.23808265C= | CA1158966170 | HMGCL | c.620G= (p.Gly207=) c.190G= c.*661G= (n.*661G=) c.407G= (p.Gly136=) n.255G= n.361-50G= | |
1 | g.23808265C>G | CA339024225 | HMGCL | c.620G>C (p.Gly207Ala) c.190G>C c.*661G>C (n.*661G>C) c.407G>C (p.Gly136Ala) n.255G>C n.361-50G>C | dbSNP |
1 | g.23808265C>T | CA339024226 | HMGCL | c.620G>A (p.Gly207Asp) c.190G>A c.*661G>A (n.*661G>A) c.407G>A (p.Gly136Asp) n.255G>A n.361-50G>A | |
1 | g.23808266del | CA2742818741 | HMGCL | c.620del (p.Gly207ValfsTer8) c.190del c.*661del (n.*661del) c.407del (p.Gly136ValfsTer8) n.255del n.361-50del | |
1 | g.23808266C>A | CA339024229 | HMGCL | c.619G>T (p.Gly207Cys) c.189G>T c.*660G>T (n.*660G>T) c.406G>T (p.Gly136Cys) n.254G>T n.361-51G>T | |
1 | g.23808266C>G | CA339024231 | HMGCL | c.619G>C (p.Gly207Arg) c.189G>C c.*660G>C (n.*660G>C) c.406G>C (p.Gly136Arg) n.254G>C n.361-51G>C | |
1 | g.23808266C>T | CA339024233 | HMGCL | c.619G>A (p.Gly207Ser) c.189G>A c.*660G>A (n.*660G>A) c.406G>A (p.Gly136Ser) n.254G>A n.361-51G>A | |
1 | g.23808267A>C | CA339024236 | HMGCL | c.618T>G (p.Ile206Met) c.188T>G c.*659T>G (n.*659T>G) c.405T>G (p.Ile135Met) n.253T>G n.361-52T>G | |
1 | g.23808267A>G | CA416621580 | HMGCL | c.618T>C (p.Ile206=) c.188T>C c.*659T>C (n.*659T>C) c.405T>C (p.Ile135=) n.253T>C n.361-52T>C | |
1 | g.23808267A>T | CA416621581 | HMGCL | c.618T>A (p.Ile206=) c.188T>A c.*659T>A (n.*659T>A) c.405T>A (p.Ile135=) n.253T>A n.361-52T>A | |
1 | g.23808268A= | CA1143686937 | HMGCL | c.617T= (p.Ile206=) c.187T= c.*658T= (n.*658T=) c.404T= (p.Ile135=) n.252T= n.361-53T= | |
1 | g.23808268A>C | CA19292156 | HMGCL | c.617T>G (p.Ile206Ser) c.187T>G c.*658T>G (n.*658T>G) c.404T>G (p.Ile135Ser) n.252T>G n.361-53T>G | dbSNP |
1 | g.23808268A>G | CA686017 | HMGCL | c.617T>C (p.Ile206Thr) c.187T>C c.*658T>C (n.*658T>C) c.404T>C (p.Ile135Thr) n.252T>C n.361-53T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808268A>T | CA339024240 | HMGCL | c.617T>A (p.Ile206Asn) c.187T>A c.*658T>A (n.*658T>A) c.404T>A (p.Ile135Asn) n.252T>A n.361-53T>A | gnomAD v4 |
1 | g.23808269T>A | CA339024254 | HMGCL | c.616A>T (p.Ile206Phe) c.186A>T c.*657A>T (n.*657A>T) c.403A>T (p.Ile135Phe) n.251A>T n.361-54A>T | |
1 | g.23808269T>C | CA339024249 | HMGCL | c.616A>G (p.Ile206Val) c.186A>G c.*657A>G (n.*657A>G) c.403A>G (p.Ile135Val) n.251A>G n.361-54A>G | |
1 | g.23808269T>G | CA339024252 | HMGCL | c.616A>C (p.Ile206Leu) c.186A>C c.*657A>C (n.*657A>C) c.403A>C (p.Ile135Leu) n.251A>C n.361-54A>C | |
1 | g.23808270G>A | CA416621590 | HMGCL | c.615C>T (p.Thr205=) c.185C>T c.*656C>T (n.*656C>T) c.402C>T (p.Thr134=) n.250C>T n.361-55C>T | |
1 | g.23808270G>C | CA416621592 | HMGCL | c.615C>G (p.Thr205=) c.185C>G c.*656C>G (n.*656C>G) c.402C>G (p.Thr134=) n.250C>G n.361-55C>G | |
1 | g.23808270G>T | CA416621594 | HMGCL | c.615C>A (p.Thr205=) c.185C>A c.*656C>A (n.*656C>A) c.402C>A (p.Thr134=) n.250C>A n.361-55C>A | |
1 | g.23808271G>A | CA339024258 | HMGCL | c.614C>T (p.Thr205Ile) c.184C>T c.*655C>T (n.*655C>T) c.401C>T (p.Thr134Ile) n.249C>T n.361-56C>T | |
1 | g.23808271G>C | CA339024260 | HMGCL | c.614C>G (p.Thr205Ser) c.184C>G c.*655C>G (n.*655C>G) c.401C>G (p.Thr134Ser) n.249C>G n.361-56C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808271G= | CA1158966171 | HMGCL | c.614C= (p.Thr205=) c.184C= c.*655C= (n.*655C=) c.401C= (p.Thr134=) n.249C= n.361-56C= | |
1 | g.23808271G>T | CA339024261 | HMGCL | c.614C>A (p.Thr205Asn) c.184C>A c.*655C>A (n.*655C>A) c.401C>A (p.Thr134Asn) n.249C>A n.361-56C>A | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808272T>A | CA339024265 | HMGCL | c.613A>T (p.Thr205Ser) c.183A>T c.*654A>T (n.*654A>T) c.400A>T (p.Thr134Ser) n.248A>T n.361-57A>T | |
1 | g.23808272T>C | CA686018 | HMGCL | c.613A>G (p.Thr205Ala) c.183A>G c.*654A>G (n.*654A>G) c.400A>G (p.Thr134Ala) n.248A>G n.361-57A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808272T>G | CA339024270 | HMGCL | c.613A>C (p.Thr205Pro) c.183A>C c.*654A>C (n.*654A>C) c.400A>C (p.Thr134Pro) n.248A>C n.361-57A>C | |
1 | g.23808272T= | CA1158966172 | HMGCL | c.613A= (p.Thr205=) c.183A= c.*654A= (n.*654A=) c.400A= (p.Thr134=) n.248A= n.361-57A= | |
1 | g.23808273G>A | CA416621598 | HMGCL | c.612C>T (p.Asp204=) c.182C>T c.*653C>T (n.*653C>T) c.399C>T (p.Asp133=) n.247C>T n.361-58C>T | |
1 | g.23808273G>C | CA339024273 | HMGCL | c.612C>G (p.Asp204Glu) c.182C>G c.*653C>G (n.*653C>G) c.399C>G (p.Asp133Glu) n.247C>G n.361-58C>G | |
1 | g.23808273G>T | CA339024276 | HMGCL | c.612C>A (p.Asp204Glu) c.182C>A c.*653C>A (n.*653C>A) c.399C>A (p.Asp133Glu) n.247C>A n.361-58C>A | |
1 | g.23808274T>A | CA339024279 | HMGCL | c.611A>T (p.Asp204Val) c.181A>T c.*652A>T (n.*652A>T) c.398A>T (p.Asp133Val) n.246A>T n.361-59A>T | |
1 | g.23808274T>C | CA339024280 | HMGCL | c.611A>G (p.Asp204Gly) c.181A>G c.*652A>G (n.*652A>G) c.398A>G (p.Asp133Gly) n.246A>G n.361-59A>G | |
1 | g.23808274T>G | CA339024283 | HMGCL | c.611A>C (p.Asp204Ala) c.181A>C c.*652A>C (n.*652A>C) c.398A>C (p.Asp133Ala) n.246A>C n.361-59A>C | |
1 | g.23808275C>A | CA339024292 | HMGCL | c.610G>T (p.Asp204Tyr) c.180G>T c.*651G>T (n.*651G>T) c.397G>T (p.Asp133Tyr) n.245G>T n.361-60G>T | dbSNP |
1 | g.23808275C= | CA1158966173 | HMGCL | c.610G= (p.Asp204=) c.180G= c.*651G= (n.*651G=) c.397G= (p.Asp133=) n.245G= n.361-60G= | |
1 | g.23808275C>G | CA339024286 | HMGCL | c.610G>C (p.Asp204His) c.180G>C c.*651G>C (n.*651G>C) c.397G>C (p.Asp133His) n.245G>C n.361-60G>C | |
1 | g.23808275C>T | CA339024289 | HMGCL | c.610G>A (p.Asp204Asn) c.180G>A c.*651G>A (n.*651G>A) c.397G>A (p.Asp133Asn) n.245G>A n.361-60G>A | gnomAD v4 |
1 | g.23808279dup | CA2644076504 | HMGCL | c.610dup (p.Asp204GlyfsTer?) c.180dup c.*651dup (n.*651dup) c.397dup (p.Asp133GlyfsTer?) n.245dup n.361-60dup | gnomAD v4 |
1 | g.23808279del | CA2573132189 | HMGCL | c.610del (p.Asp204ThrfsTer11) c.180del c.*651del (n.*651del) c.397del (p.Asp133ThrfsTer11) n.245del n.361-60del | ClinVar dbSNP |
1 | g.23808276C>A | CA416621611 | HMGCL | c.609G>T (p.Gly203=) c.179G>T c.*650G>T (n.*650G>T) c.396G>T (p.Gly132=) n.244G>T n.361-61G>T | |
1 | g.23808276C>G | CA416621607 | HMGCL | c.609G>C (p.Gly203=) c.179G>C c.*650G>C (n.*650G>C) c.396G>C (p.Gly132=) n.244G>C n.361-61G>C | |
1 | g.23808276C>T | CA416621609 | HMGCL | c.609G>A (p.Gly203=) c.179G>A c.*650G>A (n.*650G>A) c.396G>A (p.Gly132=) n.244G>A n.361-61G>A | |
1 | g.23808277C>A | CA339024301 | HMGCL | c.608G>T (p.Gly203Val) c.178G>T c.*649G>T (n.*649G>T) c.395G>T (p.Gly132Val) n.243G>T n.361-62G>T | |
1 | g.23808277C= | CA1158966174 | HMGCL | c.608G= (p.Gly203=) c.178G= c.*649G= (n.*649G=) c.395G= (p.Gly132=) n.243G= n.361-62G= | |
1 | g.23808277C>G | CA339024303 | HMGCL | c.608G>C (p.Gly203Ala) c.178G>C c.*649G>C (n.*649G>C) c.395G>C (p.Gly132Ala) n.243G>C n.361-62G>C | |
1 | g.23808277C>T | CA339024308 | HMGCL | c.608G>A (p.Gly203Glu) c.178G>A c.*649G>A (n.*649G>A) c.395G>A (p.Gly132Glu) n.243G>A n.361-62G>A | ClinVar dbSNP gnomAD v4 |
1 | g.23808278C>A | CA339024312 | HMGCL | c.607G>T (p.Gly203Trp) c.177G>T c.*648G>T (n.*648G>T) c.394G>T (p.Gly132Trp) n.242G>T n.361-63G>T | |
1 | g.23808278C>G | CA339024315 | HMGCL | c.607G>C (p.Gly203Arg) c.177G>C c.*648G>C (n.*648G>C) c.394G>C (p.Gly132Arg) n.242G>C n.361-63G>C | |
1 | g.23808278C>T | CA339024317 | HMGCL | c.607G>A (p.Gly203Arg) c.177G>A c.*648G>A (n.*648G>A) c.394G>A (p.Gly132Arg) n.242G>A n.361-63G>A | |
1 | g.23808279C>A | CA416621618 | HMGCL | c.606G>T (p.Leu202=) c.176G>T c.*647G>T (n.*647G>T) c.393G>T (p.Leu131=) n.241G>T n.361-64G>T | |
1 | g.23808279C= | CA1158966175 | HMGCL | c.606G= (p.Leu202=) c.176G= c.*647G= (n.*647G=) c.393G= (p.Leu131=) n.241G= n.361-64G= | |
1 | g.23808279C>G | CA416621619 | HMGCL | c.606G>C (p.Leu202=) c.176G>C c.*647G>C (n.*647G>C) c.393G>C (p.Leu131=) n.241G>C n.361-64G>C | |
1 | g.23808279C>T | CA416621620 | HMGCL | c.606G>A (p.Leu202=) c.176G>A c.*647G>A (n.*647G>A) c.393G>A (p.Leu131=) n.241G>A n.361-64G>A | dbSNP gnomAD v4 |
1 | g.23808280A>C | CA339024322 | HMGCL | c.605T>G (p.Leu202Arg) c.175T>G c.*646T>G (n.*646T>G) c.392T>G (p.Leu131Arg) n.240T>G n.361-65T>G | |
1 | g.23808280A>G | CA339024324 | HMGCL | c.605T>C (p.Leu202Pro) c.175T>C c.*646T>C (n.*646T>C) c.392T>C (p.Leu131Pro) n.240T>C n.361-65T>C | |
1 | g.23808280A>T | CA339024328 | HMGCL | c.605T>A (p.Leu202Gln) c.175T>A c.*646T>A (n.*646T>A) c.392T>A (p.Leu131Gln) n.240T>A n.361-65T>A | |
1 | g.23808281G>A | CA686019 | HMGCL | c.604C>T (p.Leu202=) c.174C>T c.*645C>T (n.*645C>T) c.391C>T (p.Leu131=) n.239C>T n.361-66C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.23808281G>C | CA339024333 | HMGCL | c.604C>G (p.Leu202Val) c.174C>G c.*645C>G (n.*645C>G) c.391C>G (p.Leu131Val) n.239C>G n.361-66C>G | |
1 | g.23808281G= | CA1142125591 | HMGCL | c.604C= (p.Leu202=) c.174C= c.*645C= (n.*645C=) c.391C= (p.Leu131=) n.239C= n.361-66C= | |
1 | g.23808281G>T | CA339024335 | HMGCL | c.604C>A (p.Leu202Met) c.174C>A c.*645C>A (n.*645C>A) c.391C>A (p.Leu131Met) n.239C>A n.361-66C>A | |
1 | g.23808282G>A | CA416621627 | HMGCL | c.603C>T (p.Ser201=) c.173C>T c.*644C>T (n.*644C>T) c.390C>T (p.Ser130=) n.238C>T n.361-67C>T | |
1 | g.23808282G>C | CA416621629 | HMGCL | c.603C>G (p.Ser201=) c.173C>G c.*644C>G (n.*644C>G) c.390C>G (p.Ser130=) n.238C>G n.361-67C>G | |
1 | g.23808282G>T | CA416621631 | HMGCL | c.603C>A (p.Ser201=) c.173C>A c.*644C>A (n.*644C>A) c.390C>A (p.Ser130=) n.238C>A n.361-67C>A | |
1 | g.23808283G>A | CA339024345 | HMGCL | c.602C>T (p.Ser201Phe) c.172C>T c.*643C>T (n.*643C>T) c.389C>T (p.Ser130Phe) n.237C>T n.361-68C>T | COSMIC |
1 | g.23808283G>C | CA339024343 | HMGCL | c.602C>G (p.Ser201Cys) c.172C>G c.*643C>G (n.*643C>G) c.389C>G (p.Ser130Cys) n.237C>G n.361-68C>G | |
1 | g.23808283G= | CA1158966176 | HMGCL | c.602C= (p.Ser201=) c.172C= c.*643C= (n.*643C=) c.389C= (p.Ser130=) n.237C= n.361-68C= | |
1 | g.23808283G>T | CA686020 | HMGCL | c.602C>A (p.Ser201Tyr) c.172C>A c.*643C>A (n.*643C>A) c.389C>A (p.Ser130Tyr) n.237C>A n.361-68C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.23808284A>C | CA339024356 | HMGCL | c.601T>G (p.Ser201Ala) c.171T>G c.*642T>G (n.*642T>G) c.388T>G (p.Ser130Ala) n.236T>G n.361-69T>G | |
1 | g.23808284A>G | CA339024351 | HMGCL | c.601T>C (p.Ser201Pro) c.171T>C c.*642T>C (n.*642T>C) c.388T>C (p.Ser130Pro) n.236T>C n.361-69T>C | dbSNP |
1 | g.23808284A>T | CA339024353 | HMGCL | c.601T>A (p.Ser201Thr) c.171T>A c.*642T>A (n.*642T>A) c.388T>A (p.Ser130Thr) n.236T>A n.361-69T>A | |
1 | g.23808285G>A | CA416621638 | HMGCL | c.600C>T (p.Ile200=) c.170C>T c.*641C>T (n.*641C>T) c.387C>T (p.Ile129=) n.235C>T n.361-70C>T | |
1 | g.23808285G>C | CA339024359 | HMGCL | c.600C>G (p.Ile200Met) c.170C>G c.*641C>G (n.*641C>G) c.387C>G (p.Ile129Met) n.235C>G n.361-70C>G | dbSNP gnomAD v3 gnomAD v4 |
1 | g.23808285G= | CA1158966177 | HMGCL | c.600C= (p.Ile200=) c.170C= c.*641C= (n.*641C=) c.387C= (p.Ile129=) n.235C= n.361-70C= | |
1 | g.23808285G>T | CA416621640 | HMGCL | c.600C>A (p.Ile200=) c.170C>A c.*641C>A (n.*641C>A) c.387C>A (p.Ile129=) n.235C>A n.361-70C>A | gnomAD v4 |
1 | g.23808286A>C | CA339024362 | HMGCL | c.599T>G (p.Ile200Ser) c.169T>G c.*640T>G (n.*640T>G) c.386T>G (p.Ile129Ser) n.234T>G n.361-71T>G | |
1 | g.23808286A>G | CA339024365 | HMGCL | c.599T>C (p.Ile200Thr) c.169T>C c.*640T>C (n.*640T>C) c.386T>C (p.Ile129Thr) n.234T>C n.361-71T>C | gnomAD v4 |
1 | g.23808286A>T | CA339024367 | HMGCL | c.599T>A (p.Ile200Asn) c.169T>A c.*640T>A (n.*640T>A) c.386T>A (p.Ile129Asn) n.234T>A n.361-71T>A | |
1 | g.23808287T>A | CA339024374 | HMGCL | c.598A>T (p.Ile200Phe) c.168A>T c.*639A>T (n.*639A>T) c.385A>T (p.Ile129Phe) n.233A>T n.361-72A>T | gnomAD v4 |
1 | g.23808287T>C | CA339024370 | HMGCL | c.598A>G (p.Ile200Val) c.168A>G c.*639A>G (n.*639A>G) c.385A>G (p.Ile129Val) n.233A>G n.361-72A>G | |
1 | g.23808287T>G | CA339024373 | HMGCL | c.598A>C (p.Ile200Leu) c.168A>C c.*639A>C (n.*639A>C) c.385A>C (p.Ile129Leu) n.233A>C n.361-72A>C |