Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.31598651_31598654delinsTGTC | CA2293889373 | TTR | c.420_423delinsTGTC (p.Ala140=) c.324_327delinsTGTC (p.Ala108=) c.534_537delinsTGTC (p.Ala178=) c.396_399delinsTGTC (p.Ala132=) | |
18 | g.31598655_31598657del | CA256856 | TTR | c.424_426del (p.Val142del) c.328_330del (p.Val110del) c.538_540del (p.Val180del) c.400_402del (p.Val134del) | ClinVar dbSNP |
18 | g.31598654C>A | CA503610961 | TTR | c.423C>A (p.Val141=) c.327C>A (p.Val109=) c.537C>A (p.Val179=) c.399C>A (p.Val133=) | |
18 | g.31598654C= | CA2293889374 | TTR | c.423C= (p.Val141=) c.327C= (p.Val109=) c.537C= (p.Val179=) c.399C= (p.Val133=) | |
18 | g.31598654C>G | CA503610963 | TTR | c.423C>G (p.Val141=) c.327C>G (p.Val109=) c.537C>G (p.Val179=) c.399C>G (p.Val133=) | |
18 | g.31598654C>T | CA8928513 | TTR | c.423C>T (p.Val141=) c.327C>T (p.Val109=) c.537C>T (p.Val179=) c.399C>T (p.Val133=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
18 | g.31598655G>A | CA214382 | TTR | c.424G>A (p.Val142Ile) c.328G>A (p.Val110Ile) c.538G>A (p.Val180Ile) c.400G>A (p.Val134Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.31598655G>C | CA402158279 | TTR | c.424G>C (p.Val142Leu) c.328G>C (p.Val110Leu) c.538G>C (p.Val180Leu) c.400G>C (p.Val134Leu) | |
18 | g.31598655G= | CA2293889375 | TTR | c.424G= (p.Val142=) c.328G= (p.Val110=) c.538G= (p.Val180=) c.400G= (p.Val134=) | |
18 | g.31598655G>T | CA402158278 | TTR | c.424G>T (p.Val142Phe) c.328G>T (p.Val110Phe) c.538G>T (p.Val180Phe) c.400G>T (p.Val134Phe) | |
18 | g.31598656T>A | CA402158280 | TTR | c.425T>A (p.Val142Asp) c.329T>A (p.Val110Asp) c.539T>A (p.Val180Asp) c.401T>A (p.Val134Asp) | |
18 | g.31598656T>C | CA402158281 | TTR | c.425T>C (p.Val142Ala) c.329T>C (p.Val110Ala) c.539T>C (p.Val180Ala) c.401T>C (p.Val134Ala) | ClinVar dbSNP |
18 | g.31598656T>G | CA402158282 | TTR | c.425T>G (p.Val142Gly) c.329T>G (p.Val110Gly) c.539T>G (p.Val180Gly) c.401T>G (p.Val134Gly) | |
18 | g.31598657C>A | CA503610965 | TTR | c.426C>A (p.Val142=) c.330C>A (p.Val110=) c.540C>A (p.Val180=) c.402C>A (p.Val134=) | |
18 | g.31598657C= | CA2293889376 | TTR | c.426C= (p.Val142=) c.330C= (p.Val110=) c.540C= (p.Val180=) c.402C= (p.Val134=) | |
18 | g.31598657C>G | CA503610966 | TTR | c.426C>G (p.Val142=) c.330C>G (p.Val110=) c.540C>G (p.Val180=) c.402C>G (p.Val134=) | |
18 | g.31598657C>T | CA297742017 | TTR | c.426C>T (p.Val142=) c.330C>T (p.Val110=) c.540C>T (p.Val180=) c.402C>T (p.Val134=) | dbSNP |
18 | g.31598658A>C | CA402158283 | TTR | c.427A>C (p.Thr143Pro) c.331A>C (p.Thr111Pro) c.541A>C (p.Thr181Pro) c.403A>C (p.Thr135Pro) | |
18 | g.31598658A>G | CA402158284 | TTR | c.427A>G (p.Thr143Ala) c.331A>G (p.Thr111Ala) c.541A>G (p.Thr181Ala) c.403A>G (p.Thr135Ala) | ClinVar gnomAD v4 |
18 | g.31598658A>T | CA402158285 | TTR | c.427A>T (p.Thr143Ser) c.331A>T (p.Thr111Ser) c.541A>T (p.Thr181Ser) c.403A>T (p.Thr135Ser) | gnomAD v4 |
18 | g.31598658_31598664delinsACCAATC | CA2293889377 | TTR | c.427_433delinsACCAATC (p.Thr143=) c.331_337delinsACCAATC (p.Thr111=) c.541_547delinsACCAATC (p.Thr181=) c.403_409delinsACCAATC (p.Thr135=) | |
18 | g.31598659C>A | CA402158286 | TTR | c.428C>A (p.Thr143Asn) c.332C>A (p.Thr111Asn) c.542C>A (p.Thr181Asn) c.404C>A (p.Thr135Asn) | |
18 | g.31598659C>G | CA402158287 | TTR | c.428C>G (p.Thr143Ser) c.332C>G (p.Thr111Ser) c.542C>G (p.Thr181Ser) c.404C>G (p.Thr135Ser) | |
18 | g.31598659C>T | CA402158288 | TTR | c.428C>T (p.Thr143Ile) c.332C>T (p.Thr111Ile) c.542C>T (p.Thr181Ile) c.404C>T (p.Thr135Ile) | |
18 | g.31598663_31598668del | CA10641397 | TTR | c.432_437del (p.Asn144_Pro145del) c.336_341del (p.Asn112_Pro113del) c.546_551del (p.Asn182_Pro183del) c.408_413del (p.Asn136_Pro137del) | ClinVar dbSNP |
18 | g.31598660C>A | CA503610969 | TTR | c.429C>A (p.Thr143=) c.333C>A (p.Thr111=) c.543C>A (p.Thr181=) c.405C>A (p.Thr135=) | |
18 | g.31598660C>G | CA503610970 | TTR | c.429C>G (p.Thr143=) c.333C>G (p.Thr111=) c.543C>G (p.Thr181=) c.405C>G (p.Thr135=) | |
18 | g.31598660C>T | CA503610971 | TTR | c.429C>T (p.Thr143=) c.333C>T (p.Thr111=) c.543C>T (p.Thr181=) c.405C>T (p.Thr135=) | |
18 | g.31598661A>C | CA402158291 | TTR | c.430A>C (p.Asn144His) c.334A>C (p.Asn112His) c.544A>C (p.Asn182His) c.406A>C (p.Asn136His) | |
18 | g.31598661A>G | CA402158290 | TTR | c.430A>G (p.Asn144Asp) c.334A>G (p.Asn112Asp) c.544A>G (p.Asn182Asp) c.406A>G (p.Asn136Asp) | |
18 | g.31598661A>T | CA402158289 | TTR | c.430A>T (p.Asn144Tyr) c.334A>T (p.Asn112Tyr) c.544A>T (p.Asn182Tyr) c.406A>T (p.Asn136Tyr) | |
18 | g.31598662A= | CA2293889378 | TTR | c.431A= (p.Asn144=) c.335A= (p.Asn112=) c.545A= (p.Asn182=) c.407A= (p.Asn136=) | |
18 | g.31598662A>C | CA402158292 | TTR | c.431A>C (p.Asn144Thr) c.335A>C (p.Asn112Thr) c.545A>C (p.Asn182Thr) c.407A>C (p.Asn136Thr) | |
18 | g.31598662A>G | CA8928514 | TTR | c.431A>G (p.Asn144Ser) c.335A>G (p.Asn112Ser) c.545A>G (p.Asn182Ser) c.407A>G (p.Asn136Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.31598662A>T | CA402158293 | TTR | c.431A>T (p.Asn144Ile) c.335A>T (p.Asn112Ile) c.545A>T (p.Asn182Ile) c.407A>T (p.Asn136Ile) | dbSNP |
18 | g.31598663T>A | CA402158294 | TTR | c.432T>A (p.Asn144Lys) c.336T>A (p.Asn112Lys) c.546T>A (p.Asn182Lys) c.408T>A (p.Asn136Lys) | |
18 | g.31598663T>C | CA503610972 | TTR | c.432T>C (p.Asn144=) c.336T>C (p.Asn112=) c.546T>C (p.Asn182=) c.408T>C (p.Asn136=) | |
18 | g.31598663T>G | CA402158295 | TTR | c.432T>G (p.Asn144Lys) c.336T>G (p.Asn112Lys) c.546T>G (p.Asn182Lys) c.408T>G (p.Asn136Lys) | |
18 | g.31598664C>A | CA402158296 | TTR | c.433C>A (p.Pro145Thr) c.337C>A (p.Pro113Thr) c.547C>A (p.Pro183Thr) c.409C>A (p.Pro137Thr) | dbSNP |
18 | g.31598664C= | CA2293889379 | TTR | c.433C= (p.Pro145=) c.337C= (p.Pro113=) c.547C= (p.Pro183=) c.409C= (p.Pro137=) | |
18 | g.31598664C>G | CA402158297 | TTR | c.433C>G (p.Pro145Ala) c.337C>G (p.Pro113Ala) c.547C>G (p.Pro183Ala) c.409C>G (p.Pro137Ala) | |
18 | g.31598664C>T | CA402158298 | TTR | c.433C>T (p.Pro145Ser) c.337C>T (p.Pro113Ser) c.547C>T (p.Pro183Ser) c.409C>T (p.Pro137Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
18 | g.31598665C>A | CA297742019 | TTR | c.434C>A (p.Pro145His) c.338C>A (p.Pro113His) c.548C>A (p.Pro183His) c.410C>A (p.Pro137His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
18 | g.31598665C= | CA2293889380 | TTR | c.434C= (p.Pro145=) c.338C= (p.Pro113=) c.548C= (p.Pro183=) c.410C= (p.Pro137=) | |
18 | g.31598665C>G | CA402158299 | TTR | c.434C>G (p.Pro145Arg) c.338C>G (p.Pro113Arg) c.548C>G (p.Pro183Arg) c.410C>G (p.Pro137Arg) | |
18 | g.31598665C>T | CA402158300 | TTR | c.434C>T (p.Pro145Leu) c.338C>T (p.Pro113Leu) c.548C>T (p.Pro183Leu) c.410C>T (p.Pro137Leu) | |
18 | g.31598666C>A | CA503610974 | TTR | c.435C>A (p.Pro145=) c.339C>A (p.Pro113=) c.549C>A (p.Pro183=) c.411C>A (p.Pro137=) | |
18 | g.31598666C= | CA2293889381 | TTR | c.435C= (p.Pro145=) c.339C= (p.Pro113=) c.549C= (p.Pro183=) c.411C= (p.Pro137=) | |
18 | g.31598666C>G | CA503610975 | TTR | c.435C>G (p.Pro145=) c.339C>G (p.Pro113=) c.549C>G (p.Pro183=) c.411C>G (p.Pro137=) | |
18 | g.31598666C>T | CA503610976 | TTR | c.435C>T (p.Pro145=) c.339C>T (p.Pro113=) c.549C>T (p.Pro183=) c.411C>T (p.Pro137=) | dbSNP gnomAD v2 gnomAD v4 |