Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.67940015C>A | CA396375453 | LCAT | c.1212G>T (p.Met404Ile) c.215G>T c.950G>T (n.950G>T) | |
16 | g.67940015C>G | CA396375454 | LCAT | c.1212G>C (p.Met404Ile) c.215G>C c.950G>C (n.950G>C) | |
16 | g.67940015C>T | CA396375455 | LCAT | c.1212G>A (p.Met404Ile) c.215G>A c.950G>A (n.950G>A) | |
16 | g.67940016A>C | CA396375456 | LCAT | c.1211T>G (p.Met404Arg) c.214T>G c.949T>G (n.949T>G) | |
16 | g.67940016A>G | CA396375458 | LCAT | c.1211T>C (p.Met404Thr) c.214T>C c.949T>C (n.949T>C) | gnomAD v4 |
16 | g.67940016A>T | CA396375457 | LCAT | c.1211T>A (p.Met404Lys) c.214T>A c.949T>A (n.949T>A) | |
16 | g.67940017T>A | CA396375459 | LCAT | c.1210A>T (p.Met404Leu) c.213A>T c.948A>T (n.948A>T) | |
16 | g.67940017T>C | CA8120867 | LCAT | c.1210A>G (p.Met404Val) c.213A>G c.948A>G (n.948A>G) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
16 | g.67940017T>G | CA396375460 | LCAT | c.1210A>C (p.Met404Leu) c.213A>C c.948A>C (n.948A>C) | |
16 | g.67940017T= | CA2229563167 | LCAT | c.1210A= (p.Met404=) c.213A= c.948A= (n.948A=) | |
16 | g.67940018G>A | CA496092518 | LCAT | c.1209C>T (p.Asn403=) c.212C>T c.947C>T (n.947C>T) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940018G>C | CA396375461 | LCAT | c.1209C>G (p.Asn403Lys) c.212C>G c.947C>G (n.947C>G) | |
16 | g.67940018G= | CA2229563168 | LCAT | c.1209C= (p.Asn403=) c.212C= c.947C= (n.947C=) | |
16 | g.67940018G>T | CA396375462 | LCAT | c.1209C>A (p.Asn403Lys) c.212C>A c.947C>A (n.947C>A) | |
16 | g.67940019T>A | CA396375465 | LCAT | c.1208A>T (p.Asn403Ile) c.211A>T c.946A>T (n.946A>T) | |
16 | g.67940019T>C | CA396375464 | LCAT | c.1208A>G (p.Asn403Ser) c.211A>G c.946A>G (n.946A>G) | |
16 | g.67940019T>G | CA396375463 | LCAT | c.1208A>C (p.Asn403Thr) c.211A>C c.946A>C (n.946A>C) | |
16 | g.67940020T>A | CA396375466 | LCAT | c.1207A>T (p.Asn403Tyr) c.210A>T c.945A>T (n.945A>T) | |
16 | g.67940020T>C | CA396375467 | LCAT | c.1207A>G (p.Asn403Asp) c.210A>G c.945A>G (n.945A>G) | |
16 | g.67940020T>G | CA396375468 | LCAT | c.1207A>C (p.Asn403His) c.210A>C c.945A>C (n.945A>C) | |
16 | g.67940021G>A | CA496092520 | LCAT | c.1206C>T (p.Leu402=) c.209C>T c.944C>T (n.944C>T) | |
16 | g.67940021G>C | CA496092521 | LCAT | c.1206C>G (p.Leu402=) c.209C>G c.944C>G (n.944C>G) | |
16 | g.67940021G>T | CA496092525 | LCAT | c.1206C>A (p.Leu402=) c.209C>A c.944C>A (n.944C>A) | |
16 | g.67940023_67940024del | CA2532360751 | LCAT | c.1205_1206del (p.Leu402GlnfsTer?) c.208_209del c.943_944del (n.943_944del) | |
16 | g.67940022A>C | CA396375469 | LCAT | c.1205T>G (p.Leu402Arg) c.208T>G c.943T>G (n.943T>G) | |
16 | g.67940022A>G | CA396375470 | LCAT | c.1205T>C (p.Leu402Pro) c.208T>C c.943T>C (n.943T>C) | |
16 | g.67940022A>T | CA396375471 | LCAT | c.1205T>A (p.Leu402His) c.208T>A c.943T>A (n.943T>A) | |
16 | g.67940023G>A | CA396375474 | LCAT | c.1204C>T (p.Leu402Phe) c.207C>T c.942C>T (n.942C>T) | |
16 | g.67940023G>C | CA396375472 | LCAT | c.1204C>G (p.Leu402Val) c.207C>G c.942C>G (n.942C>G) | |
16 | g.67940023G>T | CA396375473 | LCAT | c.1204C>A (p.Leu402Ile) c.207C>A c.942C>A (n.942C>A) | |
16 | g.67940024A>C | CA396375475 | LCAT | c.1203T>G (p.His401Gln) c.206T>G c.941T>G (n.941T>G) | |
16 | g.67940024A>G | CA496092533 | LCAT | c.1203T>C (p.His401=) c.206T>C c.941T>C (n.941T>C) | |
16 | g.67940024A>T | CA396375476 | LCAT | c.1203T>A (p.His401Gln) c.206T>A c.941T>A (n.941T>A) | |
16 | g.67940025T>A | CA396375477 | LCAT | c.1202A>T (p.His401Leu) c.205A>T c.940A>T (n.940A>T) | |
16 | g.67940025T>C | CA396375478 | LCAT | c.1202A>G (p.His401Arg) c.205A>G c.940A>G (n.940A>G) | |
16 | g.67940025T>G | CA396375479 | LCAT | c.1202A>C (p.His401Pro) c.205A>C c.940A>C (n.940A>C) | |
16 | g.67940026G>A | CA396375480 | LCAT | c.1201C>T (p.His401Tyr) c.204C>T c.939C>T (n.939C>T) | |
16 | g.67940026G>C | CA396375481 | LCAT | c.1201C>G (p.His401Asp) c.204C>G c.939C>G (n.939C>G) | |
16 | g.67940026G>T | CA396375482 | LCAT | c.1201C>A (p.His401Asn) c.204C>A c.939C>A (n.939C>A) | |
16 | g.67940027C>A | CA8120868 | LCAT | c.1200G>T (p.Gln400His) c.203G>T c.938G>T (n.938G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940027C= | CA2229563169 | LCAT | c.1200G= (p.Gln400=) c.203G= c.938G= (n.938G=) | |
16 | g.67940027C>G | CA396375483 | LCAT | c.1200G>C (p.Gln400His) c.203G>C c.938G>C (n.938G>C) | |
16 | g.67940027C>T | CA496092545 | LCAT | c.1200G>A (p.Gln400=) c.203G>A c.938G>A (n.938G>A) | |
16 | g.67940028T>A | CA396375484 | LCAT | c.1199A>T (p.Gln400Leu) c.202A>T c.937A>T (n.937A>T) | |
16 | g.67940028T>C | CA396375485 | LCAT | c.1199A>G (p.Gln400Arg) c.202A>G c.937A>G (n.937A>G) | |
16 | g.67940028T>G | CA396375486 | LCAT | c.1199A>C (p.Gln400Pro) c.202A>C c.937A>C (n.937A>C) | |
16 | g.67940029G>A | CA396375487 | LCAT | c.1198C>T (p.Gln400Ter) c.201C>T c.936C>T (n.936C>T) | dbSNP gnomAD v4 |
16 | g.67940029G>C | CA396375489 | LCAT | c.1198C>G (p.Gln400Glu) c.201C>G c.936C>G (n.936C>G) | |
16 | g.67940029G= | CA2229563170 | LCAT | c.1198C= (p.Gln400=) c.201C= c.936C= (n.936C=) | |
16 | g.67940029G>T | CA396375488 | LCAT | c.1198C>A (p.Gln400Lys) c.201C>A c.936C>A (n.936C>A) | |
16 | g.67940030T>A | CA496092553 | LCAT | c.1197A>T (p.Ile399=) c.200A>T c.935A>T (n.935A>T) | |
16 | g.67940030T>C | CA396375490 | LCAT | c.1197A>G (p.Ile399Met) c.200A>G c.935A>G (n.935A>G) | |
16 | g.67940030T>G | CA496092555 | LCAT | c.1197A>C (p.Ile399=) c.200A>C c.935A>C (n.935A>C) | |
16 | g.67940030dup | CA116424 | LCAT | c.1197dup (p.Gln400ThrfsTer?) c.200dup c.935dup (n.935dup) | ClinVar dbSNP |
16 | g.67940031A>C | CA396375491 | LCAT | c.1196T>G (p.Ile399Arg) c.199T>G c.934T>G (n.934T>G) | |
16 | g.67940031A>G | CA396375492 | LCAT | c.1196T>C (p.Ile399Thr) c.199T>C c.934T>C (n.934T>C) | |
16 | g.67940031A>T | CA396375493 | LCAT | c.1196T>A (p.Ile399Lys) c.199T>A c.934T>A (n.934T>A) | |
16 | g.67940032T>A | CA396375496 | LCAT | c.1195A>T (p.Ile399Leu) c.198A>T c.933A>T (n.933A>T) | |
16 | g.67940032T>C | CA396375495 | LCAT | c.1195A>G (p.Ile399Val) c.198A>G c.933A>G (n.933A>G) | |
16 | g.67940032T>G | CA396375494 | LCAT | c.1195A>C (p.Ile399Leu) c.198A>C c.933A>C (n.933A>C) | |
16 | g.67940033C>A | CA496092575 | LCAT | c.1194G>T (p.Gly398=) c.197G>T c.932G>T (n.932G>T) | |
16 | g.67940033C= | CA2229563171 | LCAT | c.1194G= (p.Gly398=) c.197G= c.932G= (n.932G=) | |
16 | g.67940033C>G | CA496092569 | LCAT | c.1194G>C (p.Gly398=) c.197G>C c.932G>C (n.932G>C) | dbSNP |
16 | g.67940033C>T | CA496092573 | LCAT | c.1194G>A (p.Gly398=) c.197G>A c.932G>A (n.932G>A) | |
16 | g.67940034C>A | CA396375497 | LCAT | c.1193G>T (p.Gly398Val) c.196G>T c.931G>T (n.931G>T) | |
16 | g.67940034C= | CA2229563172 | LCAT | c.1193G= (p.Gly398=) c.196G= c.931G= (n.931G=) | |
16 | g.67940034C>G | CA396375498 | LCAT | c.1193G>C (p.Gly398Ala) c.196G>C c.931G>C (n.931G>C) | |
16 | g.67940034C>T | CA283160392 | LCAT | c.1193G>A (p.Gly398Glu) c.196G>A c.931G>A (n.931G>A) | dbSNP gnomAD v4 |
16 | g.67940035C>A | CA396375499 | LCAT | c.1192G>T (p.Gly398Trp) c.195G>T c.930G>T (n.930G>T) | |
16 | g.67940035C= | CA2229563173 | LCAT | c.1192G= (p.Gly398=) c.195G= c.930G= (n.930G=) | |
16 | g.67940035C>G | CA396375500 | LCAT | c.1192G>C (p.Gly398Arg) c.195G>C c.930G>C (n.930G>C) | |
16 | g.67940035C>T | CA8120869 | LCAT | c.1192G>A (p.Gly398Arg) c.195G>A c.930G>A (n.930G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940036G>A | CA8120870 | LCAT | c.1191C>T (p.His397=) c.194C>T c.929C>T (n.929C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940036G>C | CA396375502 | LCAT | c.1191C>G (p.His397Gln) c.194C>G c.929C>G (n.929C>G) | |
16 | g.67940036G= | CA2229563174 | LCAT | c.1191C= (p.His397=) c.194C= c.929C= (n.929C=) | |
16 | g.67940036G>T | CA396375501 | LCAT | c.1191C>A (p.His397Gln) c.194C>A c.929C>A (n.929C>A) | |
16 | g.67940037T>A | CA396375503 | LCAT | c.1190A>T (p.His397Leu) c.193A>T c.928A>T (n.928A>T) | gnomAD v4 |
16 | g.67940037T>C | CA396375504 | LCAT | c.1190A>G (p.His397Arg) c.193A>G c.928A>G (n.928A>G) | |
16 | g.67940037T>G | CA396375505 | LCAT | c.1190A>C (p.His397Pro) c.193A>C c.928A>C (n.928A>C) | |
16 | g.67940038G>A | CA396375506 | LCAT | c.1189C>T (p.His397Tyr) c.192C>T c.927C>T (n.927C>T) | |
16 | g.67940038G>C | CA396375507 | LCAT | c.1189C>G (p.His397Asp) c.192C>G c.927C>G (n.927C>G) | gnomAD v4 |
16 | g.67940038G= | CA2229563175 | LCAT | c.1189C= (p.His397=) c.192C= c.927C= (n.927C=) | |
16 | g.67940038G>T | CA396375508 | LCAT | c.1189C>A (p.His397Asn) c.192C>A c.927C>A (n.927C>A) | dbSNP |
16 | g.67940039C>A | CA496092601 | LCAT | c.1188G>T (p.Leu396=) c.191G>T c.926G>T (n.926G>T) | |
16 | g.67940039C= | CA2229563176 | LCAT | c.1188G= (p.Leu396=) c.191G= c.926G= (n.926G=) | |
16 | g.67940039C>G | CA496092603 | LCAT | c.1188G>C (p.Leu396=) c.191G>C c.926G>C (n.926G>C) | |
16 | g.67940039C>T | CA283160393 | LCAT | c.1188G>A (p.Leu396=) c.191G>A c.926G>A (n.926G>A) | ClinVar dbSNP gnomAD v4 |
16 | g.67940040A>C | CA396375509 | LCAT | c.1187T>G (p.Leu396Arg) c.190T>G c.925T>G (n.925T>G) | gnomAD v4 |
16 | g.67940040A>G | CA396375510 | LCAT | c.1187T>C (p.Leu396Pro) c.190T>C c.925T>C (n.925T>C) | |
16 | g.67940040A>T | CA396375511 | LCAT | c.1187T>A (p.Leu396Gln) c.190T>A c.925T>A (n.925T>A) | |
16 | g.67940041G>A | CA496092618 | LCAT | c.1186C>T (p.Leu396=) c.189C>T c.924C>T (n.924C>T) | gnomAD v4 |
16 | g.67940041G>C | CA396375512 | LCAT | c.1186C>G (p.Leu396Val) c.189C>G c.924C>G (n.924C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940041G= | CA2229563177 | LCAT | c.1186C= (p.Leu396=) c.189C= c.924C= (n.924C=) | |
16 | g.67940041G>T | CA396375513 | LCAT | c.1186C>A (p.Leu396Met) c.189C>A c.924C>A (n.924C>A) | dbSNP |
16 | g.67940042G>A | CA8120871 | LCAT | c.1185C>T (p.Pro395=) c.188C>T c.923C>T (n.923C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940042G>C | CA496092624 | LCAT | c.1185C>G (p.Pro395=) c.188C>G c.923C>G (n.923C>G) | |
16 | g.67940042G= | CA2229563178 | LCAT | c.1185C= (p.Pro395=) c.188C= c.923C= (n.923C=) | |
16 | g.67940042G>T | CA496092625 | LCAT | c.1185C>A (p.Pro395=) c.188C>A c.923C>A (n.923C>A) | dbSNP gnomAD v2 |
16 | g.67940043G>A | CA396375515 | LCAT | c.1184C>T (p.Pro395Leu) c.187C>T c.922C>T (n.922C>T) | gnomAD v4 |
16 | g.67940043G>C | CA396375514 | LCAT | c.1184C>G (p.Pro395Arg) c.187C>G c.922C>G (n.922C>G) | |
16 | g.67940043G>T | CA396375516 | LCAT | c.1184C>A (p.Pro395His) c.187C>A c.922C>A (n.922C>A) | |
16 | g.67940044G>A | CA396375517 | LCAT | c.1183C>T (p.Pro395Ser) c.186C>T c.921C>T (n.921C>T) | |
16 | g.67940044G>C | CA396375519 | LCAT | c.1183C>G (p.Pro395Ala) c.186C>G c.921C>G (n.921C>G) | gnomAD v4 |
16 | g.67940044G>T | CA396375518 | LCAT | c.1183C>A (p.Pro395Thr) c.186C>A c.921C>A (n.921C>A) | |
16 | g.67940045C>A | CA283160399 | LCAT | c.1182G>T (p.Leu394=) c.185G>T c.920G>T (n.920G>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940045C= | CA2229563179 | LCAT | c.1182G= (p.Leu394=) c.185G= c.920G= (n.920G=) | |
16 | g.67940045C>G | CA496092633 | LCAT | c.1182G>C (p.Leu394=) c.185G>C c.920G>C (n.920G>C) | |
16 | g.67940045C>T | CA496092635 | LCAT | c.1182G>A (p.Leu394=) c.185G>A c.920G>A (n.920G>A) | |
16 | g.67940046A>C | CA396375520 | LCAT | c.1181T>G (p.Leu394Arg) c.184T>G c.919T>G (n.919T>G) | |
16 | g.67940046A>G | CA396375522 | LCAT | c.1181T>C (p.Leu394Pro) c.184T>C c.919T>C (n.919T>C) | |
16 | g.67940046A>T | CA396375521 | LCAT | c.1181T>A (p.Leu394Gln) c.184T>A c.919T>A (n.919T>A) | |
16 | g.67940047G>A | CA496092640 | LCAT | c.1180C>T (p.Leu394=) c.183C>T c.918C>T (n.918C>T) | gnomAD v4 |
16 | g.67940047G>C | CA396375523 | LCAT | c.1180C>G (p.Leu394Val) c.183C>G c.918C>G (n.918C>G) | |
16 | g.67940047G>T | CA396375524 | LCAT | c.1180C>A (p.Leu394Met) c.183C>A c.918C>A (n.918C>A) | |
16 | g.67940048C>A | CA496092644 | LCAT | c.1179G>T (p.Leu393=) c.182G>T c.917G>T (n.917G>T) | |
16 | g.67940048C>G | CA496092645 | LCAT | c.1179G>C (p.Leu393=) c.182G>C c.917G>C (n.917G>C) | |
16 | g.67940048C>T | CA496092648 | LCAT | c.1179G>A (p.Leu393=) c.182G>A c.917G>A (n.917G>A) | |
16 | g.67940049A>C | CA396375525 | LCAT | c.1178T>G (p.Leu393Arg) c.181T>G c.916T>G (n.916T>G) | |
16 | g.67940049A>G | CA396375526 | LCAT | c.1178T>C (p.Leu393Pro) c.181T>C c.916T>C (n.916T>C) | |
16 | g.67940049A>T | CA396375527 | LCAT | c.1178T>A (p.Leu393Gln) c.181T>A c.916T>A (n.916T>A) | |
16 | g.67940050G>A | CA8120872 | LCAT | c.1177C>T (p.Leu393=) c.180C>T c.915C>T (n.915C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940050G>C | CA396375528 | LCAT | c.1177C>G (p.Leu393Val) c.180C>G c.915C>G (n.915C>G) | |
16 | g.67940050G= | CA2229563180 | LCAT | c.1177C= (p.Leu393=) c.180C= c.915C= (n.915C=) | |
16 | g.67940050G>T | CA396375529 | LCAT | c.1177C>A (p.Leu393Met) c.180C>A c.915C>A (n.915C>A) | |
16 | g.67940051G>A | CA496092659 | LCAT | c.1176C>T (p.His392=) c.179C>T c.914C>T (n.914C>T) | dbSNP |
16 | g.67940051G>C | CA396375530 | LCAT | c.1176C>G (p.His392Gln) c.179C>G c.914C>G (n.914C>G) | |
16 | g.67940051G= | CA2229563181 | LCAT | c.1176C= (p.His392=) c.179C= c.914C= (n.914C=) | |
16 | g.67940051G>T | CA396375531 | LCAT | c.1176C>A (p.His392Gln) c.179C>A c.914C>A (n.914C>A) | |
16 | g.67940052T>A | CA396375534 | LCAT | c.1175A>T (p.His392Leu) c.178A>T c.913A>T (n.913A>T) | |
16 | g.67940052T>C | CA396375532 | LCAT | c.1175A>G (p.His392Arg) c.178A>G c.913A>G (n.913A>G) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940052T>G | CA396375533 | LCAT | c.1175A>C (p.His392Pro) c.178A>C c.913A>C (n.913A>C) | |
16 | g.67940052T= | CA2229563182 | LCAT | c.1175A= (p.His392=) c.178A= c.913A= (n.913A=) | |
16 | g.67940053G>A | CA396375535 | LCAT | c.1174C>T (p.His392Tyr) c.177C>T c.912C>T (n.912C>T) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940053G>C | CA396375536 | LCAT | c.1174C>G (p.His392Asp) c.177C>G c.912C>G (n.912C>G) | |
16 | g.67940053G= | CA2229563183 | LCAT | c.1174C= (p.His392=) c.177C= c.912C= (n.912C=) | |
16 | g.67940053G>T | CA396375537 | LCAT | c.1174C>A (p.His392Asn) c.177C>A c.912C>A (n.912C>A) | |
16 | g.67940054C>A | CA496092682 | LCAT | c.1173G>T (p.Val391=) c.176G>T c.911G>T (n.911G>T) | |
16 | g.67940054C= | CA2229563184 | LCAT | c.1173G= (p.Val391=) c.176G= c.911G= (n.911G=) | |
16 | g.67940054C>G | CA496092680 | LCAT | c.1173G>C (p.Val391=) c.176G>C c.911G>C (n.911G>C) | |
16 | g.67940054C>T | CA8120873 | LCAT | c.1173G>A (p.Val391=) c.176G>A c.911G>A (n.911G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940055A= | CA2229563185 | LCAT | c.1172T= (p.Val391=) c.175T= c.910T= (n.910T=) | |
16 | g.67940055A>C | CA396375538 | LCAT | c.1172T>G (p.Val391Gly) c.175T>G c.910T>G (n.910T>G) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940055A>G | CA8120874 | LCAT | c.1172T>C (p.Val391Ala) c.175T>C c.910T>C (n.910T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940055A>T | CA396375539 | LCAT | c.1172T>A (p.Val391Glu) c.175T>A c.910T>A (n.910T>A) | |
16 | g.67940056C>A | CA396375540 | LCAT | c.1171G>T (p.Val391Leu) c.174G>T c.909G>T (n.909G>T) | |
16 | g.67940056C>G | CA396375541 | LCAT | c.1171G>C (p.Val391Leu) c.174G>C c.909G>C (n.909G>C) | |
16 | g.67940056C>T | CA396375542 | LCAT | c.1171G>A (p.Val391Met) c.174G>A c.909G>A (n.909G>A) | |
16 | g.67940057A= | CA2229563186 | LCAT | c.1170T= (p.Pro390=) c.173T= c.908T= (n.908T=) | |
16 | g.67940057A>C | CA496092693 | LCAT | c.1170T>G (p.Pro390=) c.173T>G c.908T>G (n.908T>G) | |
16 | g.67940057A>G | CA496092696 | LCAT | c.1170T>C (p.Pro390=) c.173T>C c.908T>C (n.908T>C) | dbSNP gnomAD v4 |
16 | g.67940057A>T | CA496092697 | LCAT | c.1170T>A (p.Pro390=) c.173T>A c.908T>A (n.908T>A) | |
16 | g.67940058G>A | CA396375544 | LCAT | c.1169C>T (p.Pro390Leu) c.172C>T c.907C>T (n.907C>T) | |
16 | g.67940058G>C | CA396375545 | LCAT | c.1169C>G (p.Pro390Arg) c.172C>G c.907C>G (n.907C>G) | |
16 | g.67940058G>T | CA396375543 | LCAT | c.1169C>A (p.Pro390His) c.172C>A c.907C>A (n.907C>A) | |
16 | g.67940059G>A | CA8120875 | LCAT | c.1168C>T (p.Pro390Ser) c.171C>T c.906C>T (n.906C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940059G>C | CA396375546 | LCAT | c.1168C>G (p.Pro390Ala) c.171C>G c.906C>G (n.906C>G) | |
16 | g.67940059G= | CA2229563187 | LCAT | c.1168C= (p.Pro390=) c.171C= c.906C= (n.906C=) | |
16 | g.67940059G>T | CA396375547 | LCAT | c.1168C>A (p.Pro390Thr) c.171C>A c.906C>A (n.906C>A) | |
16 | g.67940060C>A | CA396375548 | LCAT | c.1167G>T (p.Gln389His) c.170G>T c.905G>T (n.905G>T) | |
16 | g.67940060C= | CA2229563188 | LCAT | c.1167G= (p.Gln389=) c.170G= c.905G= (n.905G=) | |
16 | g.67940060C>G | CA8120876 | LCAT | c.1167G>C (p.Gln389His) c.170G>C c.905G>C (n.905G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940060C>T | CA496092709 | LCAT | c.1167G>A (p.Gln389=) c.170G>A c.905G>A (n.905G>A) | gnomAD v4 |
16 | g.67940061T>A | CA396375551 | LCAT | c.1166A>T (p.Gln389Leu) c.169A>T c.904A>T (n.904A>T) | |
16 | g.67940061T>C | CA396375549 | LCAT | c.1166A>G (p.Gln389Arg) c.169A>G c.904A>G (n.904A>G) | |
16 | g.67940061T>G | CA396375550 | LCAT | c.1166A>C (p.Gln389Pro) c.169A>C c.904A>C (n.904A>C) | |
16 | g.67940062G>A | CA396375552 | LCAT | c.1165C>T (p.Gln389Ter) c.168C>T c.903C>T (n.903C>T) | |
16 | g.67940062G>C | CA396375553 | LCAT | c.1165C>G (p.Gln389Glu) c.168C>G c.903C>G (n.903C>G) | |
16 | g.67940062G>T | CA396375554 | LCAT | c.1165C>A (p.Gln389Lys) c.168C>A c.903C>A (n.903C>A) | |
16 | g.67940063T>A | CA496092734 | LCAT | c.1164A>T (p.Pro388=) c.167A>T c.902A>T (n.902A>T) | |
16 | g.67940063T>C | CA8120878 | LCAT | c.1164A>G (p.Pro388=) c.167A>G c.902A>G (n.902A>G) | dbSNP ExAC gnomAD v4 |
16 | g.67940063T>G | CA8120877 | LCAT | c.1164A>C (p.Pro388=) c.167A>C c.902A>C (n.902A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940063T= | CA2229563189 | LCAT | c.1164A= (p.Pro388=) c.167A= c.902A= (n.902A=) | |
16 | g.67940064G>A | CA396375555 | LCAT | c.1163C>T (p.Pro388Leu) c.166C>T c.901C>T (n.901C>T) | ClinVar dbSNP gnomAD v4 |
16 | g.67940064G>C | CA396375557 | LCAT | c.1163C>G (p.Pro388Arg) c.166C>G c.901C>G (n.901C>G) | |
16 | g.67940064G= | CA2229563190 | LCAT | c.1163C= (p.Pro388=) c.166C= c.901C= (n.901C=) | |
16 | g.67940064G>T | CA396375556 | LCAT | c.1163C>A (p.Pro388Gln) c.166C>A c.901C>A (n.901C>A) | |
16 | g.67940065G>A | CA396375558 | LCAT | c.1162C>T (p.Pro388Ser) c.165C>T c.900C>T (n.900C>T) | gnomAD v4 |
16 | g.67940065G>C | CA396375559 | LCAT | c.1162C>G (p.Pro388Ala) c.165C>G c.900C>G (n.900C>G) | |
16 | g.67940065G>T | CA396375560 | LCAT | c.1162C>A (p.Pro388Thr) c.165C>A c.900C>A (n.900C>A) | |
16 | g.67940066C>A | CA396375561 | LCAT | c.1161G>T (p.Gln387His) c.164G>T c.899G>T (n.899G>T) | gnomAD v4 |
16 | g.67940066C>G | CA396375562 | LCAT | c.1161G>C (p.Gln387His) c.164G>C c.899G>C (n.899G>C) | |
16 | g.67940066C>T | CA496092757 | LCAT | c.1161G>A (p.Gln387=) c.164G>A c.899G>A (n.899G>A) | COSMIC |
16 | g.67940067T>A | CA396375563 | LCAT | c.1160A>T (p.Gln387Leu) c.163A>T c.898A>T (n.898A>T) | |
16 | g.67940067T>C | CA396375564 | LCAT | c.1160A>G (p.Gln387Arg) c.163A>G c.898A>G (n.898A>G) | |
16 | g.67940067T>G | CA396375565 | LCAT | c.1160A>C (p.Gln387Pro) c.163A>C c.898A>C (n.898A>C) | |
16 | g.67940067T= | CA2229563191 | LCAT | c.1160A= (p.Gln387=) c.163A= c.898A= (n.898A=) | |
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 |