Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68784912G>ACA381633328CPT1Ac.1066C>T (p.Pro356Ser)
c.1162C>T (p.Pro388Ser)
11g.68784912G>CCA381633330CPT1Ac.1066C>G (p.Pro356Ala)
c.1162C>G (p.Pro388Ala)
11g.68784912G>TCA381633332CPT1Ac.1066C>A (p.Pro356Thr)
c.1162C>A (p.Pro388Thr)
11g.68784913C>ACA223375844CPT1Ac.1065G>T (p.Lys355Asn)
c.1161G>T (p.Lys387Asn)
dbSNP
11g.68784913C>GCA381633334CPT1Ac.1065G>C (p.Lys355Asn)
c.1161G>C (p.Lys387Asn)
11g.68784913C>TCA475197736CPT1Ac.1065G>A (p.Lys355=)
c.1161G>A (p.Lys387=)
ClinVar dbSNP gnomAD v4
11g.68784914T>ACA381633336CPT1Ac.1064A>T (p.Lys355Met)
c.1160A>T (p.Lys387Met)
11g.68784914T>CCA381633338CPT1Ac.1064A>G (p.Lys355Arg)
c.1160A>G (p.Lys387Arg)
11g.68784914T>GCA381633339CPT1Ac.1064A>C (p.Lys355Thr)
c.1160A>C (p.Lys387Thr)
11g.68784915T>ACA381633342CPT1Ac.1063A>T (p.Lys355Ter)
c.1159A>T (p.Lys387Ter)
gnomAD v4
11g.68784915T>CCA381633344CPT1Ac.1063A>G (p.Lys355Glu)
c.1159A>G (p.Lys387Glu)
gnomAD v4
11g.68784915T>GCA381633346CPT1Ac.1063A>C (p.Lys355Gln)
c.1159A>C (p.Lys387Gln)
11g.68784916C>ACA475197755CPT1Ac.1062G>T (p.Leu354=)
c.1158G>T (p.Leu386=)
11g.68784916C>GCA475197753CPT1Ac.1062G>C (p.Leu354=)
c.1158G>C (p.Leu386=)
11g.68784916C>TCA6152424CPT1Ac.1062G>A (p.Leu354=)
c.1158G>A (p.Leu386=)
dbSNP ExAC gnomAD v2
11g.68784917A>CCA381633348CPT1Ac.1061T>G (p.Leu354Arg)
c.1157T>G (p.Leu386Arg)
11g.68784917A>GCA381633350CPT1Ac.1061T>C (p.Leu354Pro)
c.1157T>C (p.Leu386Pro)
11g.68784917A>TCA381633352CPT1Ac.1061T>A (p.Leu354Gln)
c.1157T>A (p.Leu386Gln)
11g.68784918G>ACA475197763CPT1Ac.1060C>T (p.Leu354=)
c.1156C>T (p.Leu386=)
dbSNP
11g.68784918G>CCA381633354CPT1Ac.1060C>G (p.Leu354Val)
c.1156C>G (p.Leu386Val)
11g.68784918G>TCA381633355CPT1Ac.1060C>A (p.Leu354Met)
c.1156C>A (p.Leu386Met)
11g.68784919C>ACA475197773CPT1Ac.1059G>T (p.Leu353=)
c.1155G>T (p.Leu385=)
11g.68784919C>GCA475197771CPT1Ac.1059G>C (p.Leu353=)
c.1155G>C (p.Leu385=)
11g.68784919C>TCA475197769CPT1Ac.1059G>A (p.Leu353=)
c.1155G>A (p.Leu385=)
11g.68784920A>CCA381633360CPT1Ac.1058T>G (p.Leu353Arg)
c.1154T>G (p.Leu385Arg)
11g.68784920A>GCA6152425CPT1Ac.1058T>C (p.Leu353Pro)
c.1154T>C (p.Leu385Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.68784920A>TCA381633358CPT1Ac.1058T>A (p.Leu353Gln)
c.1154T>A (p.Leu385Gln)
11g.68784921G>ACA475197782CPT1Ac.1057C>T (p.Leu353=)
c.1153C>T (p.Leu385=)
ClinVar
11g.68784921G>CCA381633361CPT1Ac.1057C>G (p.Leu353Val)
c.1153C>G (p.Leu385Val)
11g.68784921G>TCA381633362CPT1Ac.1057C>A (p.Leu353Met)
c.1153C>A (p.Leu385Met)
11g.68784922C>ACA475197787CPT1Ac.1056G>T (p.Arg352=)
c.1152G>T (p.Arg384=)
11g.68784922C>GCA475197794CPT1Ac.1056G>C (p.Arg352=)
c.1152G>C (p.Arg384=)
11g.68784922C>TCA475197790CPT1Ac.1056G>A (p.Arg352=)
c.1152G>A (p.Arg384=)
ClinVar dbSNP
11g.68784923C>ACA381633364CPT1Ac.1055G>T (p.Arg352Leu)
c.1151G>T (p.Arg384Leu)
gnomAD v4
11g.68784923C>GCA381633367CPT1Ac.1055G>C (p.Arg352Pro)
c.1151G>C (p.Arg384Pro)
11g.68784923C>TCA6152426CPT1Ac.1055G>A (p.Arg352Gln)
c.1151G>A (p.Arg384Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68784924G>ACA6152427CPT1Ac.1054C>T (p.Arg352Trp)
c.1150C>T (p.Arg384Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68784924G>CCA381633370CPT1Ac.1054C>G (p.Arg352Gly)
c.1150C>G (p.Arg384Gly)
11g.68784924G>TCA475197816CPT1Ac.1054C>A (p.Arg352=)
c.1150C>A (p.Arg384=)
11g.68784925C>ACA475197820CPT1Ac.1053G>T (p.Gly351=)
c.1149G>T (p.Gly383=)
11g.68784925C>GCA475197822CPT1Ac.1053G>C (p.Gly351=)
c.1149G>C (p.Gly383=)
11g.68784925C>TCA475197823CPT1Ac.1053G>A (p.Gly351=)
c.1149G>A (p.Gly383=)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.68784926C>ACA381633372CPT1Ac.1052G>T (p.Gly351Val)
c.1148G>T (p.Gly383Val)
11g.68784926C>GCA381633373CPT1Ac.1052G>C (p.Gly351Ala)
c.1148G>C (p.Gly383Ala)
11g.68784926C>TCA381633374CPT1Ac.1052G>A (p.Gly351Glu)
c.1148G>A (p.Gly383Glu)
11g.68784927C>ACA381633375CPT1Ac.1051G>T (p.Gly351Trp)
c.1147G>T (p.Gly383Trp)
11g.68784927C>GCA381633376CPT1Ac.1051G>C (p.Gly351Arg)
c.1147G>C (p.Gly383Arg)
11g.68784927C>TCA381633377CPT1Ac.1051G>A (p.Gly351Arg)
c.1147G>A (p.Gly383Arg)
11g.68784928A>CCA381633379CPT1Ac.1050T>G (p.Asp350Glu)
c.1146T>G (p.Asp382Glu)
11g.68784928A>GCA6152428CPT1Ac.1050T>C (p.Asp350=)
c.1146T>C (p.Asp382=)
ClinVar dbSNP ExAC gnomAD v4

Number of alleles fetched