| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.52906068_52906071del | CA990396985 | DCC | c.437_440del (p.Thr146AsnfsTer?) c.238_241del c.368_371del (p.Thr123AsnfsTer?) c.358_361del n.350_353del c.358_361del (n.358_361del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906071A>C | CA402513520 | DCC | c.440A>C (p.Glu147Ala) c.241A>C c.371A>C (p.Glu124Ala) c.361A>C n.353A>C c.361A>C (n.361A>C) | |
| 18 | g.52906071A>G | CA402513521 | DCC | c.440A>G (p.Glu147Gly) c.241A>G c.371A>G (p.Glu124Gly) c.361A>G n.353A>G c.361A>G (n.361A>G) | |
| 18 | g.52906071A>T | CA402513519 | DCC | c.440A>T (p.Glu147Val) c.241A>T c.371A>T (p.Glu124Val) c.361A>T n.353A>T c.361A>T (n.361A>T) | COSMIC |
| 18 | g.52906072A>C | CA402513522 | DCC | c.441A>C (p.Glu147Asp) c.242A>C c.372A>C (p.Glu124Asp) c.362A>C n.354A>C c.362A>C (n.362A>C) | |
| 18 | g.52906072A>G | CA503999291 | DCC | c.441A>G (p.Glu147=) c.242A>G c.372A>G (p.Glu124=) c.362A>G n.354A>G c.362A>G (n.362A>G) | |
| 18 | g.52906072A>T | CA402513523 | DCC | c.441A>T (p.Glu147Asp) c.242A>T c.372A>T (p.Glu124Asp) c.362A>T n.354A>T c.362A>T (n.362A>T) | |
| 18 | g.52906073T>A | CA402513524 | DCC | c.442T>A (p.Ser148Thr) c.243T>A c.373T>A (p.Ser125Thr) c.363T>A n.355T>A c.363T>A (n.363T>A) | gnomAD v4 |
| 18 | g.52906073T>C | CA402513525 | DCC | c.442T>C (p.Ser148Pro) c.243T>C c.373T>C (p.Ser125Pro) c.363T>C n.355T>C c.363T>C (n.363T>C) | |
| 18 | g.52906073T>G | CA402513526 | DCC | c.442T>G (p.Ser148Ala) c.243T>G c.373T>G (p.Ser125Ala) c.363T>G n.355T>G c.363T>G (n.363T>G) | |
| 18 | g.52906074C>A | CA300657947 | DCC | c.443C>A (p.Ser148Tyr) c.244C>A c.374C>A (p.Ser125Tyr) c.364C>A n.356C>A c.364C>A (n.364C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906074C= | CA2303875012 | DCC | c.443C= (p.Ser148=) c.244C= c.374C= (p.Ser125=) c.364C= n.356C= c.364C= (n.364C=) | |
| 18 | g.52906074C>G | CA402513527 | DCC | c.443C>G (p.Ser148Cys) c.244C>G c.374C>G (p.Ser125Cys) c.364C>G n.356C>G c.364C>G (n.364C>G) | |
| 18 | g.52906074C>T | CA402513528 | DCC | c.443C>T (p.Ser148Phe) c.244C>T c.374C>T (p.Ser125Phe) c.364C>T n.356C>T c.364C>T (n.364C>T) | |
| 18 | g.52906075T>A | CA503999294 | DCC | c.444T>A (p.Ser148=) c.245T>A c.375T>A (p.Ser125=) c.365T>A n.357T>A c.365T>A (n.365T>A) | |
| 18 | g.52906075T>C | CA503999295 | DCC | c.444T>C (p.Ser148=) c.245T>C c.375T>C (p.Ser125=) c.365T>C n.357T>C c.365T>C (n.365T>C) | |
| 18 | g.52906075T>G | CA503999296 | DCC | c.444T>G (p.Ser148=) c.245T>G c.375T>G (p.Ser125=) c.365T>G n.357T>G c.365T>G (n.365T>G) | |
| 18 | g.52906076G>A | CA402513529 | DCC | c.445G>A (p.Val149Ile) c.246G>A c.376G>A (p.Val126Ile) c.366G>A n.358G>A c.366G>A (n.366G>A) | |
| 18 | g.52906076G>C | CA402513530 | DCC | c.445G>C (p.Val149Leu) c.246G>C c.376G>C (p.Val126Leu) c.366G>C n.358G>C c.366G>C (n.366G>C) | |
| 18 | g.52906076G>T | CA402513531 | DCC | c.445G>T (p.Val149Phe) c.246G>T c.376G>T (p.Val126Phe) c.366G>T n.358G>T c.366G>T (n.366G>T) | |
| 18 | g.52906077T>A | CA402513532 | DCC | c.446T>A (p.Val149Asp) c.247T>A c.377T>A (p.Val126Asp) c.367T>A n.359T>A c.367T>A (n.367T>A) | |
| 18 | g.52906077T>C | CA402513533 | DCC | c.446T>C (p.Val149Ala) c.247T>C c.377T>C (p.Val126Ala) c.367T>C n.359T>C c.367T>C (n.367T>C) | |
| 18 | g.52906077T>G | CA402513534 | DCC | c.446T>G (p.Val149Gly) c.247T>G c.377T>G (p.Val126Gly) c.367T>G n.359T>G c.367T>G (n.367T>G) | |
| 18 | g.52906078C>A | CA503999298 | DCC | c.447C>A (p.Val149=) c.248C>A c.378C>A (p.Val126=) c.368C>A n.360C>A c.368C>A (n.368C>A) | |
| 18 | g.52906078C= | CA2303875013 | DCC | c.447C= (p.Val149=) c.248C= c.378C= (p.Val126=) c.368C= n.360C= c.368C= (n.368C=) | |
| 18 | g.52906078C>G | CA503999299 | DCC | c.447C>G (p.Val149=) c.248C>G c.378C>G (p.Val126=) c.368C>G n.360C>G c.368C>G (n.368C>G) | |
| 18 | g.52906078C>T | CA8966550 | DCC | c.447C>T (p.Val149=) c.248C>T c.378C>T (p.Val126=) c.368C>T n.360C>T c.368C>T (n.368C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.52906079A>C | CA402513535 | DCC | c.448A>C (p.Thr150Pro) c.249A>C c.379A>C (p.Thr127Pro) c.369A>C n.361A>C c.369A>C (n.369A>C) | |
| 18 | g.52906079A>G | CA402513536 | DCC | c.448A>G (p.Thr150Ala) c.249A>G c.379A>G (p.Thr127Ala) c.369A>G n.361A>G c.369A>G (n.369A>G) | |
| 18 | g.52906079A>T | CA402513537 | DCC | c.448A>T (p.Thr150Ser) c.249A>T c.379A>T (p.Thr127Ser) c.369A>T n.361A>T c.369A>T (n.369A>T) | |
| 18 | g.52906080C>A | CA8966551 | DCC | c.449C>A (p.Thr150Lys) c.250C>A c.380C>A (p.Thr127Lys) c.370C>A n.362C>A c.370C>A (n.370C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.52906080C= | CA2303875014 | DCC | c.449C= (p.Thr150=) c.250C= c.380C= (p.Thr127=) c.370C= n.362C= c.370C= (n.370C=) | |
| 18 | g.52906080C>G | CA402513538 | DCC | c.449C>G (p.Thr150Arg) c.250C>G c.380C>G (p.Thr127Arg) c.370C>G n.362C>G c.370C>G (n.370C>G) | |
| 18 | g.52906080C>T | CA402513539 | DCC | c.449C>T (p.Thr150Ile) c.250C>T c.380C>T (p.Thr127Ile) c.370C>T n.362C>T c.370C>T (n.370C>T) | COSMIC |
| 18 | g.52906081A>C | CA503999300 | DCC | c.450A>C (p.Thr150=) c.251A>C c.381A>C (p.Thr127=) c.371A>C n.363A>C c.371A>C (n.371A>C) | |
| 18 | g.52906081A>G | CA503999302 | DCC | c.450A>G (p.Thr150=) c.251A>G c.381A>G (p.Thr127=) c.371A>G n.363A>G c.371A>G (n.371A>G) | |
| 18 | g.52906081A>T | CA503999301 | DCC | c.450A>T (p.Thr150=) c.251A>T c.381A>T (p.Thr127=) c.371A>T n.363A>T c.371A>T (n.371A>T) | gnomAD v4 |
| 18 | g.52906082G>A | CA402513540 | DCC | c.451G>A (p.Ala151Thr) c.252G>A c.382G>A (p.Ala128Thr) c.372G>A n.364G>A c.372G>A (n.372G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906082G>C | CA402513541 | DCC | c.451G>C (p.Ala151Pro) c.252G>C c.382G>C (p.Ala128Pro) c.372G>C n.364G>C c.372G>C (n.372G>C) | |
| 18 | g.52906082G= | CA2303875015 | DCC | c.451G= (p.Ala151=) c.252G= c.382G= (p.Ala128=) c.372G= n.364G= c.372G= (n.372G=) | |
| 18 | g.52906082G>T | CA402513542 | DCC | c.451G>T (p.Ala151Ser) c.252G>T c.382G>T (p.Ala128Ser) c.372G>T n.364G>T c.372G>T (n.372G>T) | |
| 18 | g.52906083C>A | CA402513543 | DCC | c.452C>A (p.Ala151Asp) c.253C>A c.383C>A (p.Ala128Asp) c.373C>A n.365C>A c.373C>A (n.373C>A) | COSMIC |
| 18 | g.52906083C= | CA2303875016 | DCC | c.452C= (p.Ala151=) c.253C= c.383C= (p.Ala128=) c.373C= n.365C= c.373C= (n.373C=) | |
| 18 | g.52906083C>G | CA402513544 | DCC | c.452C>G (p.Ala151Gly) c.253C>G c.383C>G (p.Ala128Gly) c.373C>G n.365C>G c.373C>G (n.373C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906083C>T | CA402513545 | DCC | c.452C>T (p.Ala151Val) c.253C>T c.383C>T (p.Ala128Val) c.373C>T n.365C>T c.373C>T (n.373C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906084C>A | CA503999303 | DCC | c.453C>A (p.Ala151=) c.254C>A c.384C>A (p.Ala128=) c.374C>A n.366C>A c.374C>A (n.374C>A) | |
| 18 | g.52906084C>G | CA503999304 | DCC | c.453C>G (p.Ala151=) c.254C>G c.384C>G (p.Ala128=) c.374C>G n.366C>G c.374C>G (n.374C>G) | |
| 18 | g.52906084C>T | CA503999305 | DCC | c.453C>T (p.Ala151=) c.254C>T c.384C>T (p.Ala128=) c.374C>T n.366C>T c.374C>T (n.374C>T) | gnomAD v4 |
| 18 | g.52906085T>A | CA402513548 | DCC | c.454T>A (p.Phe152Ile) c.255T>A c.385T>A (p.Phe129Ile) c.375T>A n.367T>A c.375T>A (n.375T>A) | |
| 18 | g.52906085T>C | CA402513547 | DCC | c.454T>C (p.Phe152Leu) c.255T>C c.385T>C (p.Phe129Leu) c.375T>C n.367T>C c.375T>C (n.375T>C) | |
| 18 | g.52906085T>G | CA402513546 | DCC | c.454T>G (p.Phe152Val) c.255T>G c.385T>G (p.Phe129Val) c.375T>G n.367T>G c.375T>G (n.375T>G) | gnomAD v4 |
| 18 | g.52906086T>A | CA402513549 | DCC | c.455T>A (p.Phe152Tyr) c.256T>A c.386T>A (p.Phe129Tyr) c.376T>A n.368T>A c.376T>A (n.376T>A) | |
| 18 | g.52906086T>C | CA402513551 | DCC | c.455T>C (p.Phe152Ser) c.256T>C c.386T>C (p.Phe129Ser) c.376T>C n.368T>C c.376T>C (n.376T>C) | |
| 18 | g.52906086T>G | CA402513550 | DCC | c.455T>G (p.Phe152Cys) c.256T>G c.386T>G (p.Phe129Cys) c.376T>G n.368T>G c.376T>G (n.376T>G) | |
| 18 | g.52906087C>A | CA402513552 | DCC | c.456C>A (p.Phe152Leu) c.257C>A c.387C>A (p.Phe129Leu) c.377C>A n.369C>A c.377C>A (n.377C>A) | |
| 18 | g.52906087C= | CA2303875017 | DCC | c.456C= (p.Phe152=) c.257C= c.387C= (p.Phe129=) c.377C= n.369C= c.377C= (n.377C=) | |
| 18 | g.52906087C>G | CA402513553 | DCC | c.456C>G (p.Phe152Leu) c.257C>G c.387C>G (p.Phe129Leu) c.377C>G n.369C>G c.377C>G (n.377C>G) | COSMIC |
| 18 | g.52906087C>T | CA8966552 | DCC | c.456C>T (p.Phe152=) c.257C>T c.387C>T (p.Phe129=) c.377C>T n.369C>T c.377C>T (n.377C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.52906088A>C | CA402513554 | DCC | c.457A>C (p.Met153Leu) c.258A>C c.388A>C (p.Met130Leu) c.378A>C n.370A>C c.378A>C (n.378A>C) | |
| 18 | g.52906088A>G | CA402513556 | DCC | c.457A>G (p.Met153Val) c.258A>G c.388A>G (p.Met130Val) c.378A>G n.370A>G c.378A>G (n.378A>G) | |
| 18 | g.52906088A>T | CA402513555 | DCC | c.457A>T (p.Met153Leu) c.258A>T c.388A>T (p.Met130Leu) c.378A>T n.370A>T c.378A>T (n.378A>T) | |
| 18 | g.52906089T>A | CA402513557 | DCC | c.458T>A (p.Met153Lys) c.259T>A c.389T>A (p.Met130Lys) c.379T>A n.371T>A c.379T>A (n.379T>A) | |
| 18 | g.52906089T>C | CA402513559 | DCC | c.458T>C (p.Met153Thr) c.259T>C c.389T>C (p.Met130Thr) c.379T>C n.371T>C c.379T>C (n.379T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906089T>G | CA402513558 | DCC | c.458T>G (p.Met153Arg) c.259T>G c.389T>G (p.Met130Arg) c.379T>G n.371T>G c.379T>G (n.379T>G) | |
| 18 | g.52906089T= | CA2303875018 | DCC | c.458T= (p.Met153=) c.259T= c.389T= (p.Met130=) c.379T= n.371T= c.379T= (n.379T=) | |
| 18 | g.52906090G>A | CA402513560 | DCC | c.459G>A (p.Met153Ile) c.260G>A c.390G>A (p.Met130Ile) c.380G>A n.372G>A c.380G>A (n.380G>A) | |
| 18 | g.52906090G>C | CA402513561 | DCC | c.459G>C (p.Met153Ile) c.260G>C c.390G>C (p.Met130Ile) c.380G>C n.372G>C c.380G>C (n.380G>C) | |
| 18 | g.52906090G>T | CA402513562 | DCC | c.459G>T (p.Met153Ile) c.260G>T c.390G>T (p.Met130Ile) c.380G>T n.372G>T c.380G>T (n.380G>T) | |
| 18 | g.52906091G>A | CA402513563 | DCC | c.460G>A (p.Gly154Arg) c.261G>A c.391G>A (p.Gly131Arg) c.381G>A n.373G>A c.381G>A (n.381G>A) | |
| 18 | g.52906091G>C | CA402513564 | DCC | c.460G>C (p.Gly154Arg) c.261G>C c.391G>C (p.Gly131Arg) c.381G>C n.373G>C c.381G>C (n.381G>C) | |
| 18 | g.52906091G>T | CA402513565 | DCC | c.460G>T (p.Gly154Ter) c.261G>T c.391G>T (p.Gly131Ter) c.381G>T n.373G>T c.381G>T (n.381G>T) | COSMIC |
| 18 | g.52906092G>A | CA402513566 | DCC | c.461G>A (p.Gly154Glu) c.262G>A c.392G>A (p.Gly131Glu) c.382G>A n.374G>A c.382G>A (n.382G>A) | |
| 18 | g.52906092G>C | CA8966553 | DCC | c.461G>C (p.Gly154Ala) c.262G>C c.392G>C (p.Gly131Ala) c.382G>C n.374G>C c.382G>C (n.382G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.52906092G= | CA2303875019 | DCC | c.461G= (p.Gly154=) c.262G= c.392G= (p.Gly131=) c.382G= n.374G= c.382G= (n.382G=) | |
| 18 | g.52906092G>T | CA402513567 | DCC | c.461G>T (p.Gly154Val) c.262G>T c.392G>T (p.Gly131Val) c.382G>T n.374G>T c.382G>T (n.382G>T) | |
| 18 | g.52906093A= | CA2303875020 | DCC | c.462A= (p.Gly154=) c.263A= c.393A= (p.Gly131=) c.383A= n.375A= c.383A= (n.383A=) | |
| 18 | g.52906093A>C | CA503999306 | DCC | c.462A>C (p.Gly154=) c.263A>C c.393A>C (p.Gly131=) c.383A>C n.375A>C c.383A>C (n.383A>C) | |
| 18 | g.52906093A>G | CA503999307 | DCC | c.462A>G (p.Gly154=) c.263A>G c.393A>G (p.Gly131=) c.383A>G n.375A>G c.383A>G (n.383A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.52906093A>T | CA503999308 | DCC | c.462A>T (p.Gly154=) c.263A>T c.393A>T (p.Gly131=) c.383A>T n.375A>T c.383A>T (n.383A>T) | |
| 18 | g.52906094G>A | CA402513570 | DCC | c.463G>A (p.Asp155Asn) c.264G>A c.394G>A (p.Asp132Asn) c.384G>A n.376G>A c.384G>A (n.384G>A) | COSMIC COSMIC |
| 18 | g.52906094G>C | CA402513569 | DCC | c.463G>C (p.Asp155His) c.264G>C c.394G>C (p.Asp132His) c.384G>C n.376G>C c.384G>C (n.384G>C) | |
| 18 | g.52906094G>T | CA402513568 | DCC | c.463G>T (p.Asp155Tyr) c.264G>T c.394G>T (p.Asp132Tyr) c.384G>T n.376G>T c.384G>T (n.384G>T) | |
| 18 | g.52906095A>C | CA402513571 | DCC | c.464A>C (p.Asp155Ala) c.265A>C c.395A>C (p.Asp132Ala) c.385A>C n.377A>C c.385A>C (n.385A>C) | |
| 18 | g.52906095A>G | CA402513572 | DCC | c.464A>G (p.Asp155Gly) c.265A>G c.395A>G (p.Asp132Gly) c.385A>G n.377A>G c.385A>G (n.385A>G) | |
| 18 | g.52906095A>T | CA402513573 | DCC | c.464A>T (p.Asp155Val) c.265A>T c.395A>T (p.Asp132Val) c.385A>T n.377A>T c.385A>T (n.385A>T) | |
| 18 | g.52906096C>A | CA402513574 | DCC | c.465C>A (p.Asp155Glu) c.266C>A c.396C>A (p.Asp132Glu) c.386C>A n.378C>A c.386C>A (n.386C>A) | |
| 18 | g.52906096C= | CA2303875021 | DCC | c.465C= (p.Asp155=) c.266C= c.396C= (p.Asp132=) c.386C= n.378C= c.386C= (n.386C=) | |
| 18 | g.52906096C>G | CA402513575 | DCC | c.465C>G (p.Asp155Glu) c.266C>G c.396C>G (p.Asp132Glu) c.386C>G n.378C>G c.386C>G (n.386C>G) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 18 | g.52906096C>T | CA300657948 | DCC | c.465C>T (p.Asp155=) c.266C>T c.396C>T (p.Asp132=) c.386C>T n.378C>T c.386C>T (n.386C>T) | dbSNP |
| 18 | g.52906097A= | CA2303875022 | DCC | c.466A= (p.Thr156=) c.267A= c.397A= (p.Thr133=) c.387A= n.379A= c.387A= (n.387A=) | |
| 18 | g.52906097A>C | CA402513576 | DCC | c.466A>C (p.Thr156Pro) c.267A>C c.397A>C (p.Thr133Pro) c.387A>C n.379A>C c.387A>C (n.387A>C) | gnomAD v4 |
| 18 | g.52906097A>G | CA8966554 | DCC | c.466A>G (p.Thr156Ala) c.267A>G c.397A>G (p.Thr133Ala) c.387A>G n.379A>G c.387A>G (n.387A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906097A>T | CA402513577 | DCC | c.466A>T (p.Thr156Ser) c.267A>T c.397A>T (p.Thr133Ser) c.387A>T n.379A>T c.387A>T (n.387A>T) | |
| 18 | g.52906098C>A | CA402513578 | DCC | c.467C>A (p.Thr156Lys) c.268C>A c.398C>A (p.Thr133Lys) c.388C>A n.380C>A c.388C>A (n.388C>A) | gnomAD v4 |
| 18 | g.52906098C>G | CA402513579 | DCC | c.467C>G (p.Thr156Arg) c.268C>G c.398C>G (p.Thr133Arg) c.388C>G n.380C>G c.388C>G (n.388C>G) | gnomAD v4 COSMIC COSMIC |
| 18 | g.52906098C>T | CA402513580 | DCC | c.467C>T (p.Thr156Ile) c.268C>T c.398C>T (p.Thr133Ile) c.388C>T n.380C>T c.388C>T (n.388C>T) | gnomAD v4 |
| 18 | g.52906099A>C | CA503999311 | DCC | c.468A>C (p.Thr156=) c.269A>C c.399A>C (p.Thr133=) c.389A>C n.381A>C c.389A>C (n.389A>C) | |
| 18 | g.52906099A>G | CA503999312 | DCC | c.468A>G (p.Thr156=) c.269A>G c.399A>G (p.Thr133=) c.389A>G n.381A>G c.389A>G (n.389A>G) | |
| 18 | g.52906099A>T | CA503999313 | DCC | c.468A>T (p.Thr156=) c.269A>T c.399A>T (p.Thr133=) c.389A>T n.381A>T c.389A>T (n.389A>T) | gnomAD v4 |
| 18 | g.52906100G>A | CA8966555 | DCC | c.469G>A (p.Val157Met) c.270G>A c.400G>A (p.Val134Met) c.390G>A n.382G>A c.390G>A (n.390G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.52906100G>C | CA402513582 | DCC | c.469G>C (p.Val157Leu) c.270G>C c.400G>C (p.Val134Leu) c.390G>C n.382G>C c.390G>C (n.390G>C) | gnomAD v4 |
| 18 | g.52906100G= | CA2303875023 | DCC | c.469G= (p.Val157=) c.270G= c.400G= (p.Val134=) c.390G= n.382G= c.390G= (n.390G=) | |
| 18 | g.52906100G>T | CA402513581 | DCC | c.469G>T (p.Val157Leu) c.270G>T c.400G>T (p.Val134Leu) c.390G>T n.382G>T c.390G>T (n.390G>T) | |
| 18 | g.52906101T>A | CA402513583 | DCC | c.470T>A (p.Val157Glu) c.271T>A c.401T>A (p.Val134Glu) c.391T>A n.383T>A c.391T>A (n.391T>A) | |
| 18 | g.52906101T>C | CA402513584 | DCC | c.470T>C (p.Val157Ala) c.271T>C c.401T>C (p.Val134Ala) c.391T>C n.383T>C c.391T>C (n.391T>C) | |
| 18 | g.52906101T>G | CA402513585 | DCC | c.470T>G (p.Val157Gly) c.271T>G c.401T>G (p.Val134Gly) c.391T>G n.383T>G c.391T>G (n.391T>G) | |
| 18 | g.52906102G>A | CA503999317 | DCC | c.471G>A (p.Val157=) c.272G>A c.402G>A (p.Val134=) c.392G>A n.384G>A c.392G>A (n.392G>A) | gnomAD v4 |
| 18 | g.52906102G>C | CA503999319 | DCC | c.471G>C (p.Val157=) c.272G>C c.402G>C (p.Val134=) c.392G>C n.384G>C c.392G>C (n.392G>C) | |
| 18 | g.52906102G>T | CA503999320 | DCC | c.471G>T (p.Val157=) c.272G>T c.402G>T (p.Val134=) c.392G>T n.384G>T c.392G>T (n.392G>T) | |
| 18 | g.52906103C>A | CA402513586 | DCC | c.472C>A (p.Leu158Ile) c.273C>A c.403C>A (p.Leu135Ile) c.393C>A n.385C>A c.393C>A (n.393C>A) | |
| 18 | g.52906103C>G | CA402513587 | DCC | c.472C>G (p.Leu158Val) c.273C>G c.403C>G (p.Leu135Val) c.393C>G n.385C>G c.393C>G (n.393C>G) | |
| 18 | g.52906103C>T | CA503999321 | DCC | c.472C>T (p.Leu158=) c.273C>T c.403C>T (p.Leu135=) c.393C>T n.385C>T c.393C>T (n.393C>T) | |
| 18 | g.52906104T>A | CA402513588 | DCC | c.473T>A (p.Leu158Gln) c.274T>A c.404T>A (p.Leu135Gln) c.394T>A n.386T>A c.394T>A (n.394T>A) | |
| 18 | g.52906104T>C | CA402513589 | DCC | c.473T>C (p.Leu158Pro) c.274T>C c.404T>C (p.Leu135Pro) c.394T>C n.386T>C c.394T>C (n.394T>C) | |
| 18 | g.52906104T>G | CA402513590 | DCC | c.473T>G (p.Leu158Arg) c.274T>G c.404T>G (p.Leu135Arg) c.394T>G n.386T>G c.394T>G (n.394T>G) | |
| 18 | g.52906105A= | CA2303875024 | DCC | c.474A= (p.Leu158=) c.275A= c.405A= (p.Leu135=) c.395A= n.387A= c.395A= (n.395A=) | |
| 18 | g.52906105A>C | CA8966556 | DCC | c.474A>C (p.Leu158=) c.275A>C c.405A>C (p.Leu135=) c.395A>C n.387A>C c.395A>C (n.395A>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906105A>G | CA503999322 | DCC | c.474A>G (p.Leu158=) c.275A>G c.405A>G (p.Leu135=) c.395A>G n.387A>G c.395A>G (n.395A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.52906105A>T | CA503999323 | DCC | c.474A>T (p.Leu158=) c.275A>T c.405A>T (p.Leu135=) c.395A>T n.387A>T c.395A>T (n.395A>T) | |
| 18 | g.52906106C>A | CA402513591 | DCC | c.475C>A (p.Leu159Ile) c.276C>A c.406C>A (p.Leu136Ile) c.396C>A n.388C>A c.396C>A (n.396C>A) | gnomAD v4 |
| 18 | g.52906106C>G | CA402513592 | DCC | c.475C>G (p.Leu159Val) c.276C>G c.406C>G (p.Leu136Val) c.396C>G n.388C>G c.396C>G (n.396C>G) | |
| 18 | g.52906106C>T | CA402513593 | DCC | c.475C>T (p.Leu159Phe) c.276C>T c.406C>T (p.Leu136Phe) c.396C>T n.388C>T c.396C>T (n.396C>T) | gnomAD v4 |
| 18 | g.52906107T>A | CA402513596 | DCC | c.476T>A (p.Leu159His) c.277T>A c.407T>A (p.Leu136His) c.397T>A n.389T>A c.397T>A (n.397T>A) | |
| 18 | g.52906107T>C | CA402513594 | DCC | c.476T>C (p.Leu159Pro) c.277T>C c.407T>C (p.Leu136Pro) c.397T>C n.389T>C c.397T>C (n.397T>C) | |
| 18 | g.52906107T>G | CA402513595 | DCC | c.476T>G (p.Leu159Arg) c.277T>G c.407T>G (p.Leu136Arg) c.397T>G n.389T>G c.397T>G (n.397T>G) | |
| 18 | g.52906108C>A | CA503999324 | DCC | c.477C>A (p.Leu159=) c.278C>A c.408C>A (p.Leu136=) c.398C>A n.390C>A c.398C>A (n.398C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906108C= | CA2303875025 | DCC | c.477C= (p.Leu159=) c.278C= c.408C= (p.Leu136=) c.398C= n.390C= c.398C= (n.398C=) | |
| 18 | g.52906108C>G | CA503999325 | DCC | c.477C>G (p.Leu159=) c.278C>G c.408C>G (p.Leu136=) c.398C>G n.390C>G c.398C>G (n.398C>G) | dbSNP |
| 18 | g.52906108C>T | CA503999326 | DCC | c.477C>T (p.Leu159=) c.278C>T c.408C>T (p.Leu136=) c.398C>T n.390C>T c.398C>T (n.398C>T) | dbSNP gnomAD v4 |
| 18 | g.52906109A= | CA2303875026 | DCC | c.478A= (p.Lys160=) c.279A= c.409A= (p.Lys137=) c.399A= n.391A= c.399A= (n.399A=) | |
| 18 | g.52906109A>C | CA300657949 | DCC | c.478A>C (p.Lys160Gln) c.279A>C c.409A>C (p.Lys137Gln) c.399A>C n.391A>C c.399A>C (n.399A>C) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.52906109A>G | CA402513597 | DCC | c.478A>G (p.Lys160Glu) c.279A>G c.409A>G (p.Lys137Glu) c.399A>G n.391A>G c.399A>G (n.399A>G) | |
| 18 | g.52906109A>T | CA402513598 | DCC | c.478A>T (p.Lys160Ter) c.279A>T c.409A>T (p.Lys137Ter) c.399A>T n.391A>T c.399A>T (n.399A>T) | |
| 18 | g.52906110A>C | CA402513599 | DCC | c.479A>C (p.Lys160Thr) c.280A>C c.410A>C (p.Lys137Thr) c.400A>C n.392A>C c.400A>C (n.400A>C) | |
| 18 | g.52906110A>G | CA402513600 | DCC | c.479A>G (p.Lys160Arg) c.280A>G c.410A>G (p.Lys137Arg) c.400A>G n.392A>G c.400A>G (n.400A>G) | |
| 18 | g.52906110A>T | CA402513601 | DCC | c.479A>T (p.Lys160Met) c.280A>T c.410A>T (p.Lys137Met) c.400A>T n.392A>T c.400A>T (n.400A>T) | |
| 18 | g.52906111G>A | CA503999327 | DCC | c.480G>A (p.Lys160=) c.281G>A c.411G>A (p.Lys137=) c.401G>A n.393G>A c.401G>A (n.401G>A) | dbSNP gnomAD v2 |
| 18 | g.52906111G>C | CA402513602 | DCC | c.480G>C (p.Lys160Asn) c.281G>C c.411G>C (p.Lys137Asn) c.401G>C n.393G>C c.401G>C (n.401G>C) | |
| 18 | g.52906111G= | CA2303875027 | DCC | c.480G= (p.Lys160=) c.281G= c.411G= (p.Lys137=) c.401G= n.393G= c.401G= (n.401G=) | |
| 18 | g.52906111G>T | CA402513603 | DCC | c.480G>T (p.Lys160Asn) c.281G>T c.411G>T (p.Lys137Asn) c.401G>T n.393G>T c.401G>T (n.401G>T) | |
| 18 | g.52906112T>A | CA402513604 | DCC | c.481T>A (p.Cys161Ser) c.282T>A c.412T>A (p.Cys138Ser) c.402T>A n.394T>A c.402T>A (n.402T>A) | |
| 18 | g.52906112T>C | CA402513605 | DCC | c.481T>C (p.Cys161Arg) c.282T>C c.412T>C (p.Cys138Arg) c.402T>C n.394T>C c.402T>C (n.402T>C) | |
| 18 | g.52906112T>G | CA402513606 | DCC | c.481T>G (p.Cys161Gly) c.282T>G c.412T>G (p.Cys138Gly) c.402T>G n.394T>G c.402T>G (n.402T>G) | |
| 18 | g.52906113G>A | CA402513609 | DCC | c.482G>A (p.Cys161Tyr) c.283G>A c.413G>A (p.Cys138Tyr) c.403G>A n.395G>A c.403G>A (n.403G>A) | gnomAD v4 |
| 18 | g.52906113G>C | CA402513608 | DCC | c.482G>C (p.Cys161Ser) c.283G>C c.413G>C (p.Cys138Ser) c.403G>C n.395G>C c.403G>C (n.403G>C) | |
| 18 | g.52906113G>T | CA402513607 | DCC | c.482G>T (p.Cys161Phe) c.283G>T c.413G>T (p.Cys138Phe) c.403G>T n.395G>T c.403G>T (n.403G>T) | COSMIC COSMIC |
| 18 | g.52906114T>A | CA402513610 | DCC | c.483T>A (p.Cys161Ter) c.284T>A c.414T>A (p.Cys138Ter) c.404T>A n.396T>A c.404T>A (n.404T>A) | |
| 18 | g.52906114T>C | CA503999328 | DCC | c.483T>C (p.Cys161=) c.284T>C c.414T>C (p.Cys138=) c.404T>C n.396T>C c.404T>C (n.404T>C) | |
| 18 | g.52906114T>G | CA402513611 | DCC | c.483T>G (p.Cys161Trp) c.284T>G c.414T>G (p.Cys138Trp) c.404T>G n.396T>G c.404T>G (n.404T>G) | |
| 18 | g.52906115G>A | CA300657950 | DCC | c.484G>A (p.Glu162Lys) c.285G>A c.415G>A (p.Glu139Lys) c.405G>A n.397G>A c.405G>A (n.405G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906115G>C | CA402513612 | DCC | c.484G>C (p.Glu162Gln) c.285G>C c.415G>C (p.Glu139Gln) c.405G>C n.397G>C c.405G>C (n.405G>C) | |
| 18 | g.52906115G= | CA2303875028 | DCC | c.484G= (p.Glu162=) c.285G= c.415G= (p.Glu139=) c.405G= n.397G= c.405G= (n.405G=) | |
| 18 | g.52906115G>T | CA402513613 | DCC | c.484G>T (p.Glu162Ter) c.285G>T c.415G>T (p.Glu139Ter) c.405G>T n.397G>T c.405G>T (n.405G>T) | |
| 18 | g.52906116A>C | CA402513614 | DCC | c.485A>C (p.Glu162Ala) c.286A>C c.416A>C (p.Glu139Ala) c.406A>C n.398A>C c.406A>C (n.406A>C) | |
| 18 | g.52906116A>G | CA402513615 | DCC | c.485A>G (p.Glu162Gly) c.286A>G c.416A>G (p.Glu139Gly) c.406A>G n.398A>G c.406A>G (n.406A>G) | gnomAD v4 |
| 18 | g.52906116A>T | CA402513616 | DCC | c.485A>T (p.Glu162Val) c.286A>T c.416A>T (p.Glu139Val) c.406A>T n.398A>T c.406A>T (n.406A>T) | |
| 18 | g.52906117A>C | CA402513617 | DCC | c.486A>C (p.Glu162Asp) c.287A>C c.417A>C (p.Glu139Asp) c.407A>C n.399A>C c.407A>C (n.407A>C) | |
| 18 | g.52906117A>G | CA503999329 | DCC | c.486A>G (p.Glu162=) c.287A>G c.417A>G (p.Glu139=) c.407A>G n.399A>G c.407A>G (n.407A>G) | |
| 18 | g.52906117A>T | CA402513618 | DCC | c.486A>T (p.Glu162Asp) c.287A>T c.417A>T (p.Glu139Asp) c.407A>T n.399A>T c.407A>T (n.407A>T) | |
| 18 | g.52906118G>A | CA402513619 | DCC | c.487G>A (p.Val163Ile) c.288G>A c.418G>A (p.Val140Ile) c.408G>A n.400G>A c.408G>A (n.408G>A) | |
| 18 | g.52906118G>C | CA402513620 | DCC | c.487G>C (p.Val163Leu) c.288G>C c.418G>C (p.Val140Leu) c.408G>C n.400G>C c.408G>C (n.408G>C) | |
| 18 | g.52906118G>T | CA402513621 | DCC | c.487G>T (p.Val163Phe) c.288G>T c.418G>T (p.Val140Phe) c.408G>T n.400G>T c.408G>T (n.408G>T) | |
| 18 | g.52906119T>A | CA402513624 | DCC | c.488T>A (p.Val163Asp) c.289T>A c.419T>A (p.Val140Asp) c.409T>A n.401T>A c.409T>A (n.409T>A) | |
| 18 | g.52906119T>C | CA402513623 | DCC | c.488T>C (p.Val163Ala) c.289T>C c.419T>C (p.Val140Ala) c.409T>C n.401T>C c.409T>C (n.409T>C) | dbSNP gnomAD v4 |
| 18 | g.52906119T>G | CA402513622 | DCC | c.488T>G (p.Val163Gly) c.289T>G c.419T>G (p.Val140Gly) c.409T>G n.401T>G c.409T>G (n.409T>G) | |
| 18 | g.52906119T= | CA2303875029 | DCC | c.488T= (p.Val163=) c.289T= c.419T= (p.Val140=) c.409T= n.401T= c.409T= (n.409T=) | |
| 18 | g.52906120C>A | CA503999330 | DCC | c.489C>A (p.Val163=) c.290C>A c.420C>A (p.Val140=) c.410C>A n.402C>A c.410C>A (n.410C>A) | dbSNP |
| 18 | g.52906120C= | CA2303875030 | DCC | c.489C= (p.Val163=) c.290C= c.420C= (p.Val140=) c.410C= n.402C= c.410C= (n.410C=) | |
| 18 | g.52906120C>G | CA503999331 | DCC | c.489C>G (p.Val163=) c.290C>G c.420C>G (p.Val140=) c.410C>G n.402C>G c.410C>G (n.410C>G) | |
| 18 | g.52906120C>T | CA503999332 | DCC | c.489C>T (p.Val163=) c.290C>T c.420C>T (p.Val140=) c.410C>T n.402C>T c.410C>T (n.410C>T) | |
| 18 | g.52906121A= | CA2303875031 | DCC | c.490A= (p.Ile164=) c.291A= c.421A= (p.Ile141=) c.411A= n.403A= c.411A= (n.411A=) | |
| 18 | g.52906121A>C | CA402513625 | DCC | c.490A>C (p.Ile164Leu) c.291A>C c.421A>C (p.Ile141Leu) c.411A>C n.403A>C c.411A>C (n.411A>C) | |
| 18 | g.52906121A>G | CA402513626 | DCC | c.490A>G (p.Ile164Val) c.291A>G c.421A>G (p.Ile141Val) c.411A>G n.403A>G c.411A>G (n.411A>G) | dbSNP gnomAD v4 |
| 18 | g.52906121A>T | CA402513627 | DCC | c.490A>T (p.Ile164Phe) c.291A>T c.421A>T (p.Ile141Phe) c.411A>T n.403A>T c.411A>T (n.411A>T) | |
| 18 | g.52906122T>A | CA402513628 | DCC | c.491T>A (p.Ile164Asn) c.292T>A c.422T>A (p.Ile141Asn) c.412T>A n.404T>A c.412T>A (n.412T>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906122T>C | CA8966557 | DCC | c.491T>C (p.Ile164Thr) c.292T>C c.422T>C (p.Ile141Thr) c.412T>C n.404T>C c.412T>C (n.412T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906122T>G | CA402513629 | DCC | c.491T>G (p.Ile164Ser) c.292T>G c.422T>G (p.Ile141Ser) c.412T>G n.404T>G c.412T>G (n.412T>G) | |
| 18 | g.52906122T= | CA2303875032 | DCC | c.491T= (p.Ile164=) c.292T= c.422T= (p.Ile141=) c.412T= n.404T= c.412T= (n.412T=) | |
| 18 | g.52906123T>A | CA503999333 | DCC | c.492T>A (p.Ile164=) c.293T>A c.423T>A (p.Ile141=) c.413T>A n.405T>A c.413T>A (n.413T>A) | |
| 18 | g.52906123T>C | CA503999334 | DCC | c.492T>C (p.Ile164=) c.293T>C c.423T>C (p.Ile141=) c.413T>C n.405T>C c.413T>C (n.413T>C) | |
| 18 | g.52906123T>G | CA402513630 | DCC | c.492T>G (p.Ile164Met) c.293T>G c.423T>G (p.Ile141Met) c.413T>G n.405T>G c.413T>G (n.413T>G) | |
| 18 | g.52906124G>A | CA402513631 | DCC | c.493G>A (p.Gly165Arg) c.294G>A c.424G>A (p.Gly142Arg) c.414G>A n.406G>A c.414G>A (n.414G>A) | |
| 18 | g.52906124G>C | CA402513632 | DCC | c.493G>C (p.Gly165Arg) c.294G>C c.424G>C (p.Gly142Arg) c.414G>C n.406G>C c.414G>C (n.414G>C) | |
| 18 | g.52906124G>T | CA402513633 | DCC | c.493G>T (p.Gly165Trp) c.294G>T c.424G>T (p.Gly142Trp) c.414G>T n.406G>T c.414G>T (n.414G>T) | |
| 18 | g.52906125G>A | CA402513634 | DCC | c.494G>A (p.Gly165Glu) c.295G>A c.425G>A (p.Gly142Glu) c.415G>A n.407G>A c.415G>A (n.415G>A) | |
| 18 | g.52906125G>C | CA402513635 | DCC | c.494G>C (p.Gly165Ala) c.295G>C c.425G>C (p.Gly142Ala) c.415G>C n.407G>C c.415G>C (n.415G>C) | |
| 18 | g.52906125G>T | CA402513636 | DCC | c.494G>T (p.Gly165Val) c.295G>T c.425G>T (p.Gly142Val) c.415G>T n.407G>T c.415G>T (n.415G>T) | |
| 18 | g.52906126G>A | CA503999335 | DCC | c.495G>A (p.Gly165=) c.296G>A c.426G>A (p.Gly142=) c.416G>A n.408G>A c.416G>A (n.416G>A) | |
| 18 | g.52906126G>C | CA503999336 | DCC | c.495G>C (p.Gly165=) c.296G>C c.426G>C (p.Gly142=) c.416G>C n.408G>C c.416G>C (n.416G>C) | |
| 18 | g.52906126G>T | CA503999337 | DCC | c.495G>T (p.Gly165=) c.296G>T c.426G>T (p.Gly142=) c.416G>T n.408G>T c.416G>T (n.416G>T) | |
| 18 | g.52906127G>A | CA402513638 | DCC | c.496G>A (p.Glu166Lys) c.297G>A c.427G>A (p.Glu143Lys) c.417G>A n.409G>A c.417G>A (n.417G>A) | gnomAD v4 |
| 18 | g.52906127G>C | CA402513639 | DCC | c.496G>C (p.Glu166Gln) c.297G>C c.427G>C (p.Glu143Gln) c.417G>C n.409G>C c.417G>C (n.417G>C) | |
| 18 | g.52906127G>T | CA402513637 | DCC | c.496G>T (p.Glu166Ter) c.297G>T c.427G>T (p.Glu143Ter) c.417G>T n.409G>T c.417G>T (n.417G>T) | |
| 18 | g.52906128A= | CA2303875033 | DCC | c.497A= (p.Glu166=) c.298A= c.428A= (p.Glu143=) c.418A= n.410A= c.418A= (n.418A=) | |
| 18 | g.52906128A>C | CA402513640 | DCC | c.497A>C (p.Glu166Ala) c.298A>C c.428A>C (p.Glu143Ala) c.418A>C n.410A>C c.418A>C (n.418A>C) | |
| 18 | g.52906128A>G | CA8966558 | DCC | c.497A>G (p.Glu166Gly) c.298A>G c.428A>G (p.Glu143Gly) c.418A>G n.410A>G c.418A>G (n.418A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906128A>T | CA402513641 | DCC | c.497A>T (p.Glu166Val) c.298A>T c.428A>T (p.Glu143Val) c.418A>T n.410A>T c.418A>T (n.418A>T) | |
| 18 | g.52906129G>A | CA503999338 | DCC | c.498G>A (p.Glu166=) c.299G>A c.429G>A (p.Glu143=) c.419G>A n.411G>A c.419G>A (n.419G>A) | gnomAD v4 |
| 18 | g.52906129G>C | CA402513642 | DCC | c.498G>C (p.Glu166Asp) c.299G>C c.429G>C (p.Glu143Asp) c.419G>C n.411G>C c.419G>C (n.419G>C) | |
| 18 | g.52906129G>T | CA402513643 | DCC | c.498G>T (p.Glu166Asp) c.299G>T c.429G>T (p.Glu143Asp) c.419G>T n.411G>T c.419G>T (n.419G>T) | |
| 18 | g.52906130C>A | CA402513644 | DCC | c.499C>A (p.Pro167Thr) c.300C>A c.430C>A (p.Pro144Thr) c.420C>A n.412C>A c.420C>A (n.420C>A) | |
| 18 | g.52906130C>G | CA402513645 | DCC | c.499C>G (p.Pro167Ala) c.300C>G c.430C>G (p.Pro144Ala) c.420C>G n.412C>G c.420C>G (n.420C>G) | |
| 18 | g.52906130C>T | CA402513646 | DCC | c.499C>T (p.Pro167Ser) c.300C>T c.430C>T (p.Pro144Ser) c.420C>T n.412C>T c.420C>T (n.420C>T) | |
| 18 | g.52906131C>A | CA402513647 | DCC | c.500C>A (p.Pro167His) c.301C>A c.431C>A (p.Pro144His) c.421C>A n.413C>A c.421C>A (n.421C>A) | |
| 18 | g.52906131C>G | CA402513648 | DCC | c.500C>G (p.Pro167Arg) c.301C>G c.431C>G (p.Pro144Arg) c.421C>G n.413C>G c.421C>G (n.421C>G) | |
| 18 | g.52906131C>T | CA402513649 | DCC | c.500C>T (p.Pro167Leu) c.301C>T c.431C>T (p.Pro144Leu) c.421C>T n.413C>T c.421C>T (n.421C>T) | |
| 18 | g.52906132C>A | CA503999339 | DCC | c.501C>A (p.Pro167=) c.302C>A c.432C>A (p.Pro144=) c.422C>A n.414C>A c.422C>A (n.422C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906132C= | CA2303875034 | DCC | c.501C= (p.Pro167=) c.302C= c.432C= (p.Pro144=) c.422C= n.414C= c.422C= (n.422C=) | |
| 18 | g.52906132C>G | CA503999340 | DCC | c.501C>G (p.Pro167=) c.302C>G c.432C>G (p.Pro144=) c.422C>G n.414C>G c.422C>G (n.422C>G) | |
| 18 | g.52906132C>T | CA503999341 | DCC | c.501C>T (p.Pro167=) c.302C>T c.432C>T (p.Pro144=) c.422C>T n.414C>T c.422C>T (n.422C>T) | dbSNP COSMIC COSMIC |
| 18 | g.52906133A= | CA2303875035 | DCC | c.502A= (p.Met168=) c.303A= c.433A= (p.Met145=) c.423A= n.415A= c.423A= (n.423A=) | |
| 18 | g.52906133A>C | CA402513652 | DCC | c.502A>C (p.Met168Leu) c.303A>C c.433A>C (p.Met145Leu) c.423A>C n.415A>C c.423A>C (n.423A>C) | |
| 18 | g.52906133A>G | CA402513651 | DCC | c.502A>G (p.Met168Val) c.303A>G c.433A>G (p.Met145Val) c.423A>G n.415A>G c.423A>G (n.423A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906133A>T | CA402513650 | DCC | c.502A>T (p.Met168Leu) c.303A>T c.433A>T (p.Met145Leu) c.423A>T n.415A>T c.423A>T (n.423A>T) | |
| 18 | g.52906134T>A | CA402513653 | DCC | c.503T>A (p.Met168Lys) c.304T>A c.434T>A (p.Met145Lys) c.424T>A n.416T>A c.424T>A (n.424T>A) | |
| 18 | g.52906134T>C | CA127073 | DCC | c.503T>C (p.Met168Thr) c.304T>C c.434T>C (p.Met145Thr) c.424T>C n.416T>C c.424T>C (n.424T>C) | ClinVar dbSNP |
| 18 | g.52906134T>G | CA402513654 | DCC | c.503T>G (p.Met168Arg) c.304T>G c.434T>G (p.Met145Arg) c.424T>G n.416T>G c.424T>G (n.424T>G) | |
| 18 | g.52906134T= | CA2303875036 | DCC | c.503T= (p.Met168=) c.304T= c.434T= (p.Met145=) c.424T= n.416T= c.424T= (n.424T=) | |
| 18 | g.52906135G>A | CA402513655 | DCC | c.504G>A (p.Met168Ile) c.305G>A c.435G>A (p.Met145Ile) c.425G>A n.417G>A c.425G>A (n.425G>A) | |
| 18 | g.52906135G>C | CA402513656 | DCC | c.504G>C (p.Met168Ile) c.305G>C c.435G>C (p.Met145Ile) c.425G>C n.417G>C c.425G>C (n.425G>C) | |
| 18 | g.52906135G>T | CA402513657 | DCC | c.504G>T (p.Met168Ile) c.305G>T c.435G>T (p.Met145Ile) c.425G>T n.417G>T c.425G>T (n.425G>T) | |
| 18 | g.52906136C>A | CA402513658 | DCC | c.505C>A (p.Pro169Thr) c.306C>A c.436C>A (p.Pro146Thr) c.426C>A n.418C>A c.426C>A (n.426C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906136C= | CA2303875037 | DCC | c.505C= (p.Pro169=) c.306C= c.436C= (p.Pro146=) c.426C= n.418C= c.426C= (n.426C=) | |
| 18 | g.52906136C>G | CA402513659 | DCC | c.505C>G (p.Pro169Ala) c.306C>G c.436C>G (p.Pro146Ala) c.426C>G n.418C>G c.426C>G (n.426C>G) | |
| 18 | g.52906136C>T | CA402513660 | DCC | c.505C>T (p.Pro169Ser) c.306C>T c.436C>T (p.Pro146Ser) c.426C>T n.418C>T c.426C>T (n.426C>T) | gnomAD v4 |
| 18 | g.52906137C>A | CA402513661 | DCC | c.506C>A (p.Pro169Gln) c.307C>A c.437C>A (p.Pro146Gln) c.427C>A n.419C>A c.427C>A (n.427C>A) | |
| 18 | g.52906137C>G | CA402513662 | DCC | c.506C>G (p.Pro169Arg) c.307C>G c.437C>G (p.Pro146Arg) c.427C>G n.419C>G c.427C>G (n.427C>G) | |
| 18 | g.52906137C>T | CA402513663 | DCC | c.506C>T (p.Pro169Leu) c.307C>T c.437C>T (p.Pro146Leu) c.427C>T n.419C>T c.427C>T (n.427C>T) | |
| 18 | g.52906138A= | CA2303875038 | DCC | c.507A= (p.Pro169=) c.308A= c.438A= (p.Pro146=) c.428A= n.420A= c.428A= (n.428A=) | |
| 18 | g.52906138A>C | CA503999344 | DCC | c.507A>C (p.Pro169=) c.308A>C c.438A>C (p.Pro146=) c.428A>C n.420A>C c.428A>C (n.428A>C) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.52906138A>G | CA503999342 | DCC | c.507A>G (p.Pro169=) c.308A>G c.438A>G (p.Pro146=) c.428A>G n.420A>G c.428A>G (n.428A>G) | gnomAD v4 |
| 18 | g.52906138A>T | CA503999343 | DCC | c.507A>T (p.Pro169=) c.308A>T c.438A>T (p.Pro146=) c.428A>T n.420A>T c.428A>T (n.428A>T) | |
| 18 | g.52906139A= | CA2303875039 | DCC | c.508A= (p.Thr170=) c.309A= c.439A= (p.Thr147=) c.429A= n.421A= c.429A= (n.429A=) | |
| 18 | g.52906139A>C | CA402513665 | DCC | c.508A>C (p.Thr170Pro) c.309A>C c.439A>C (p.Thr147Pro) c.429A>C n.421A>C c.429A>C (n.429A>C) | |
| 18 | g.52906139A>G | CA402513666 | DCC | c.508A>G (p.Thr170Ala) c.309A>G c.439A>G (p.Thr147Ala) c.429A>G n.421A>G c.429A>G (n.429A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906139A>T | CA402513664 | DCC | c.508A>T (p.Thr170Ser) c.309A>T c.439A>T (p.Thr147Ser) c.429A>T n.421A>T c.429A>T (n.429A>T) | |
| 18 | g.52906140C>A | CA402513667 | DCC | c.509C>A (p.Thr170Lys) c.310C>A c.440C>A (p.Thr147Lys) c.430C>A n.422C>A c.430C>A (n.430C>A) | gnomAD v4 |
| 18 | g.52906140C= | CA2303875040 | DCC | c.509C= (p.Thr170=) c.310C= c.440C= (p.Thr147=) c.430C= n.422C= c.430C= (n.430C=) | |
| 18 | g.52906140C>G | CA402513668 | DCC | c.509C>G (p.Thr170Arg) c.310C>G c.440C>G (p.Thr147Arg) c.430C>G n.422C>G c.430C>G (n.430C>G) | |
| 18 | g.52906140C>T | CA402513669 | DCC | c.509C>T (p.Thr170Ile) c.310C>T c.440C>T (p.Thr147Ile) c.430C>T n.422C>T c.430C>T (n.430C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.52906141A>C | CA503999345 | DCC | c.510A>C (p.Thr170=) c.311A>C c.441A>C (p.Thr147=) c.431A>C n.423A>C c.431A>C (n.431A>C) | |
| 18 | g.52906141A>G | CA503999346 | DCC | c.510A>G (p.Thr170=) c.311A>G c.441A>G (p.Thr147=) c.431A>G n.423A>G c.431A>G (n.431A>G) | |
| 18 | g.52906141A>T | CA503999347 | DCC | c.510A>T (p.Thr170=) c.311A>T c.441A>T (p.Thr147=) c.431A>T n.423A>T c.431A>T (n.431A>T) | |
| 18 | g.52906142A= | CA2303875041 | DCC | c.511A= (p.Ile171=) c.312A= c.442A= (p.Ile148=) c.432A= n.424A= c.432A= (n.432A=) | |
| 18 | g.52906142A>C | CA402513670 | DCC | c.511A>C (p.Ile171Leu) c.312A>C c.442A>C (p.Ile148Leu) c.432A>C n.424A>C c.432A>C (n.432A>C) | |
| 18 | g.52906142A>G | CA8966559 | DCC | c.511A>G (p.Ile171Val) c.312A>G c.442A>G (p.Ile148Val) c.432A>G n.424A>G c.432A>G (n.432A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906142A>T | CA402513671 | DCC | c.511A>T (p.Ile171Phe) c.312A>T c.442A>T (p.Ile148Phe) c.432A>T n.424A>T c.432A>T (n.432A>T) | |
| 18 | g.52906143T>A | CA402513672 | DCC | c.512T>A (p.Ile171Asn) c.313T>A c.443T>A (p.Ile148Asn) c.433T>A n.425T>A c.433T>A (n.433T>A) | |
| 18 | g.52906143T>C | CA402513673 | DCC | c.512T>C (p.Ile171Thr) c.313T>C c.443T>C (p.Ile148Thr) c.433T>C n.425T>C c.433T>C (n.433T>C) | |
| 18 | g.52906143T>G | CA402513674 | DCC | c.512T>G (p.Ile171Ser) c.313T>G c.443T>G (p.Ile148Ser) c.433T>G n.425T>G c.433T>G (n.433T>G) | |
| 18 | g.52906144C>A | CA8966561 | DCC | c.513C>A (p.Ile171=) c.314C>A c.444C>A (p.Ile148=) c.434C>A n.426C>A c.434C>A (n.434C>A) | dbSNP ExAC gnomAD v4 |
| 18 | g.52906144C= | CA2303875042 | DCC | c.513C= (p.Ile171=) c.314C= c.444C= (p.Ile148=) c.434C= n.426C= c.434C= (n.434C=) | |
| 18 | g.52906144C>G | CA402513675 | DCC | c.513C>G (p.Ile171Met) c.314C>G c.444C>G (p.Ile148Met) c.434C>G n.426C>G c.434C>G (n.434C>G) | |
| 18 | g.52906144C>T | CA8966560 | DCC | c.513C>T (p.Ile171=) c.314C>T c.444C>T (p.Ile148=) c.434C>T n.426C>T c.434C>T (n.434C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906145C>A | CA402513678 | DCC | c.514C>A (p.His172Asn) c.315C>A c.445C>A (p.His149Asn) c.435C>A n.427C>A c.435C>A (n.435C>A) | |
| 18 | g.52906145C>G | CA402513677 | DCC | c.514C>G (p.His172Asp) c.315C>G c.445C>G (p.His149Asp) c.435C>G n.427C>G c.435C>G (n.435C>G) | |
| 18 | g.52906145C>T | CA402513676 | DCC | c.514C>T (p.His172Tyr) c.315C>T c.445C>T (p.His149Tyr) c.435C>T n.427C>T c.435C>T (n.435C>T) | |
| 18 | g.52906146A>C | CA402513679 | DCC | c.515A>C (p.His172Pro) c.316A>C c.446A>C (p.His149Pro) c.436A>C n.428A>C c.436A>C (n.436A>C) | |
| 18 | g.52906146A>G | CA402513680 | DCC | c.515A>G (p.His172Arg) c.316A>G c.446A>G (p.His149Arg) c.436A>G n.428A>G c.436A>G (n.436A>G) | gnomAD v4 |
| 18 | g.52906146A>T | CA402513681 | DCC | c.515A>T (p.His172Leu) c.316A>T c.446A>T (p.His149Leu) c.436A>T n.428A>T c.436A>T (n.436A>T) | |
| 18 | g.52906147C>A | CA402513682 | DCC | c.516C>A (p.His172Gln) c.317C>A c.447C>A (p.His149Gln) c.437C>A n.429C>A c.437C>A (n.437C>A) | |
| 18 | g.52906147C>G | CA402513683 | DCC | c.516C>G (p.His172Gln) c.317C>G c.447C>G (p.His149Gln) c.437C>G n.429C>G c.437C>G (n.437C>G) | |
| 18 | g.52906147C>T | CA503999348 | DCC | c.516C>T (p.His172=) c.317C>T c.447C>T (p.His149=) c.437C>T n.429C>T c.437C>T (n.437C>T) | |
| 18 | g.52906148T>A | CA402513684 | DCC | c.517T>A (p.Trp173Arg) c.318T>A c.448T>A (p.Trp150Arg) c.438T>A n.430T>A c.438T>A (n.438T>A) | |
| 18 | g.52906148T>C | CA402513685 | DCC | c.517T>C (p.Trp173Arg) c.318T>C c.448T>C (p.Trp150Arg) c.438T>C n.430T>C c.438T>C (n.438T>C) | |
| 18 | g.52906148T>G | CA402513686 | DCC | c.517T>G (p.Trp173Gly) c.318T>G c.448T>G (p.Trp150Gly) c.438T>G n.430T>G c.438T>G (n.438T>G) | |
| 18 | g.52906149G>A | CA402513687 | DCC | c.518G>A (p.Trp173Ter) c.319G>A c.449G>A (p.Trp150Ter) c.439G>A n.431G>A c.439G>A (n.439G>A) | |
| 18 | g.52906149G>C | CA402513688 | DCC | c.518G>C (p.Trp173Ser) c.319G>C c.449G>C (p.Trp150Ser) c.439G>C n.431G>C c.439G>C (n.439G>C) | |
| 18 | g.52906149G>T | CA402513689 | DCC | c.518G>T (p.Trp173Leu) c.319G>T c.449G>T (p.Trp150Leu) c.439G>T n.431G>T c.439G>T (n.439G>T) | |
| 18 | g.52906150G>A | CA402513690 | DCC | c.519G>A (p.Trp173Ter) c.320G>A c.450G>A (p.Trp150Ter) c.440G>A n.432G>A c.440G>A (n.440G>A) | gnomAD v4 |
| 18 | g.52906150G>C | CA402513691 | DCC | c.519G>C (p.Trp173Cys) c.320G>C c.450G>C (p.Trp150Cys) c.440G>C n.432G>C c.440G>C (n.440G>C) | |
| 18 | g.52906150G>T | CA402513692 | DCC | c.519G>T (p.Trp173Cys) c.320G>T c.450G>T (p.Trp150Cys) c.440G>T n.432G>T c.440G>T (n.440G>T) | |
| 18 | g.52906151C>A | CA402513695 | DCC | c.520C>A (p.Gln174Lys) c.321C>A c.451C>A (p.Gln151Lys) c.441C>A n.433C>A c.441C>A (n.441C>A) | |
| 18 | g.52906151C>G | CA402513694 | DCC | c.520C>G (p.Gln174Glu) c.321C>G c.451C>G (p.Gln151Glu) c.441C>G n.433C>G c.441C>G (n.441C>G) | |
| 18 | g.52906151C>T | CA402513693 | DCC | c.520C>T (p.Gln174Ter) c.321C>T c.451C>T (p.Gln151Ter) c.441C>T n.433C>T c.441C>T (n.441C>T) | |
| 18 | g.52906152A>C | CA402513696 | DCC | c.521A>C (p.Gln174Pro) c.322A>C c.452A>C (p.Gln151Pro) c.442A>C n.434A>C c.442A>C (n.442A>C) | |
| 18 | g.52906152A>G | CA402513697 | DCC | c.521A>G (p.Gln174Arg) c.322A>G c.452A>G (p.Gln151Arg) c.442A>G n.434A>G c.442A>G (n.442A>G) | |
| 18 | g.52906152A>T | CA402513698 | DCC | c.521A>T (p.Gln174Leu) c.322A>T c.452A>T (p.Gln151Leu) c.442A>T n.434A>T c.442A>T (n.442A>T) | |
| 18 | g.52906153G>A | CA503999349 | DCC | c.522G>A (p.Gln174=) c.323G>A c.453G>A (p.Gln151=) c.443G>A n.435G>A c.443G>A (n.443G>A) | |
| 18 | g.52906153G>C | CA402513699 | DCC | c.522G>C (p.Gln174His) c.323G>C c.453G>C (p.Gln151His) c.443G>C n.435G>C c.443G>C (n.443G>C) | |
| 18 | g.52906153G>T | CA402513700 | DCC | c.522G>T (p.Gln174His) c.323G>T c.453G>T (p.Gln151His) c.443G>T n.435G>T c.443G>T (n.443G>T) | |
| 18 | g.52906154A>C | CA402513701 | DCC | c.523A>C (p.Lys175Gln) c.324A>C c.454A>C (p.Lys152Gln) c.444A>C n.436A>C c.444A>C (n.444A>C) | |
| 18 | g.52906154A>G | CA402513702 | DCC | c.523A>G (p.Lys175Glu) c.324A>G c.454A>G (p.Lys152Glu) c.444A>G n.436A>G c.444A>G (n.444A>G) | |
| 18 | g.52906154A>T | CA402513703 | DCC | c.523A>T (p.Lys175Ter) c.324A>T c.454A>T (p.Lys152Ter) c.444A>T n.436A>T c.444A>T (n.444A>T) | |
| 18 | g.52906155A>C | CA402513704 | DCC | c.524A>C (p.Lys175Thr) c.325A>C c.455A>C (p.Lys152Thr) c.445A>C n.437A>C c.445A>C (n.445A>C) | |
| 18 | g.52906155A>G | CA402513705 | DCC | c.524A>G (p.Lys175Arg) c.325A>G c.455A>G (p.Lys152Arg) c.445A>G n.437A>G c.445A>G (n.445A>G) | |
| 18 | g.52906155A>T | CA402513706 | DCC | c.524A>T (p.Lys175Met) c.325A>T c.455A>T (p.Lys152Met) c.445A>T n.437A>T c.445A>T (n.445A>T) | |
| 18 | g.52906156G>A | CA503999350 | DCC | c.525G>A (p.Lys175=) c.326G>A c.456G>A (p.Lys152=) c.446G>A n.438G>A c.446G>A (n.446G>A) | gnomAD v4 |
| 18 | g.52906156G>C | CA402513707 | DCC | c.525G>C (p.Lys175Asn) c.326G>C c.456G>C (p.Lys152Asn) c.446G>C n.438G>C c.446G>C (n.446G>C) | |
| 18 | g.52906156G>T | CA402513708 | DCC | c.525G>T (p.Lys175Asn) c.326G>T c.456G>T (p.Lys152Asn) c.446G>T n.438G>T c.446G>T (n.446G>T) | |
| 18 | g.52906157A= | CA2303875043 | DCC | c.526A= (p.Asn176=) c.327A= c.457A= (p.Asn153=) c.447A= n.439A= c.447A= (n.447A=) | |
| 18 | g.52906157A>C | CA402513710 | DCC | c.526A>C (p.Asn176His) c.327A>C c.457A>C (p.Asn153His) c.447A>C n.439A>C c.447A>C (n.447A>C) | |
| 18 | g.52906157A>G | CA8966562 | DCC | c.526A>G (p.Asn176Asp) c.327A>G c.457A>G (p.Asn153Asp) c.447A>G n.439A>G c.447A>G (n.447A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906157A>T | CA402513709 | DCC | c.526A>T (p.Asn176Tyr) c.327A>T c.457A>T (p.Asn153Tyr) c.447A>T n.439A>T c.447A>T (n.447A>T) | |
| 18 | g.52906158A= | CA2303875044 | DCC | c.527A= (p.Asn176=) c.328A= c.458A= (p.Asn153=) c.448A= n.440A= c.448A= (n.448A=) | |
| 18 | g.52906158A>C | CA402513711 | DCC | c.527A>C (p.Asn176Thr) c.328A>C c.458A>C (p.Asn153Thr) c.448A>C n.440A>C c.448A>C (n.448A>C) | |
| 18 | g.52906158A>G | CA347146 | DCC | c.527A>G (p.Asn176Ser) c.328A>G c.458A>G (p.Asn153Ser) c.448A>G n.440A>G c.448A>G (n.448A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.52906158A>T | CA402513712 | DCC | c.527A>T (p.Asn176Ile) c.328A>T c.458A>T (p.Asn153Ile) c.448A>T n.440A>T c.448A>T (n.448A>T) | |
| 18 | g.52906159C>A | CA8966563 | DCC | c.528C>A (p.Asn176Lys) c.329C>A c.459C>A (p.Asn153Lys) c.449C>A n.441C>A c.449C>A (n.449C>A) | dbSNP ExAC gnomAD v2 COSMIC COSMIC |
| 18 | g.52906159C= | CA2303875045 | DCC | c.528C= (p.Asn176=) c.329C= c.459C= (p.Asn153=) c.449C= n.441C= c.449C= (n.449C=) | |
| 18 | g.52906159C>G | CA402513713 | DCC | c.528C>G (p.Asn176Lys) c.329C>G c.459C>G (p.Asn153Lys) c.449C>G n.441C>G c.449C>G (n.449C>G) | |
| 18 | g.52906159C>T | CA503999351 | DCC | c.528C>T (p.Asn176=) c.329C>T c.459C>T (p.Asn153=) c.449C>T n.441C>T c.449C>T (n.449C>T) | |
| 18 | g.52906160C>A | CA402513714 | DCC | c.529C>A (p.Gln177Lys) c.330C>A c.460C>A (p.Gln154Lys) c.450C>A n.442C>A c.450C>A (n.450C>A) | dbSNP gnomAD v4 |
| 18 | g.52906160C= | CA2303875046 | DCC | c.529C= (p.Gln177=) c.330C= c.460C= (p.Gln154=) c.450C= n.442C= c.450C= (n.450C=) | |
| 18 | g.52906160C>G | CA402513716 | DCC | c.529C>G (p.Gln177Glu) c.330C>G c.460C>G (p.Gln154Glu) c.450C>G n.442C>G c.450C>G (n.450C>G) | |
| 18 | g.52906160C>T | CA402513717 | DCC | c.529C>T (p.Gln177Ter) c.330C>T c.460C>T (p.Gln154Ter) c.450C>T n.442C>T c.450C>T (n.450C>T) | |
| 18 | g.52906163_52906165del | CA2576506471 | DCC | c.532_534del (p.Gln178del) c.333_335del c.463_465del (p.Gln155del) c.453_455del n.445_447del c.453_455del (n.453_455del) | |
| 18 | g.52906161A>C | CA402513718 | DCC | c.530A>C (p.Gln177Pro) c.331A>C c.461A>C (p.Gln154Pro) c.451A>C n.443A>C c.451A>C (n.451A>C) | |
| 18 | g.52906161A>G | CA402513719 | DCC | c.530A>G (p.Gln177Arg) c.331A>G c.461A>G (p.Gln154Arg) c.451A>G n.443A>G c.451A>G (n.451A>G) | |
| 18 | g.52906161A>T | CA402513720 | DCC | c.530A>T (p.Gln177Leu) c.331A>T c.461A>T (p.Gln154Leu) c.451A>T n.443A>T c.451A>T (n.451A>T) | |
| 18 | g.52906162A>C | CA402513721 | DCC | c.531A>C (p.Gln177His) c.332A>C c.462A>C (p.Gln154His) c.452A>C n.444A>C c.452A>C (n.452A>C) | gnomAD v4 |
| 18 | g.52906162A>G | CA503999352 | DCC | c.531A>G (p.Gln177=) c.332A>G c.462A>G (p.Gln154=) c.452A>G n.444A>G c.452A>G (n.452A>G) | |
| 18 | g.52906162A>T | CA402513722 | DCC | c.531A>T (p.Gln177His) c.332A>T c.462A>T (p.Gln154His) c.452A>T n.444A>T c.452A>T (n.452A>T) | |
| 18 | g.52906163C>A | CA402513724 | DCC | c.532C>A (p.Gln178Lys) c.333C>A c.463C>A (p.Gln155Lys) c.453C>A n.445C>A c.453C>A (n.453C>A) | dbSNP |
| 18 | g.52906163C= | CA2303875047 | DCC | c.532C= (p.Gln178=) c.333C= c.463C= (p.Gln155=) c.453C= n.445C= c.453C= (n.453C=) | |
| 18 | g.52906163C>G | CA402513725 | DCC | c.532C>G (p.Gln178Glu) c.333C>G c.463C>G (p.Gln155Glu) c.453C>G n.445C>G c.453C>G (n.453C>G) | ClinVar |
| 18 | g.52906163C>T | CA402513723 | DCC | c.532C>T (p.Gln178Ter) c.333C>T c.463C>T (p.Gln155Ter) c.453C>T n.445C>T c.453C>T (n.453C>T) | |
| 18 | g.52906164A>C | CA402513726 | DCC | c.533A>C (p.Gln178Pro) c.334A>C c.464A>C (p.Gln155Pro) c.454A>C n.446A>C c.454A>C (n.454A>C) | |
| 18 | g.52906164A>G | CA402513727 | DCC | c.533A>G (p.Gln178Arg) c.334A>G c.464A>G (p.Gln155Arg) c.454A>G n.446A>G c.454A>G (n.454A>G) | gnomAD v4 |
| 18 | g.52906164A>T | CA402513728 | DCC | c.533A>T (p.Gln178Leu) c.334A>T c.464A>T (p.Gln155Leu) c.454A>T n.446A>T c.454A>T (n.454A>T) | |
| 18 | g.52906165A>C | CA402513729 | DCC | c.534A>C (p.Gln178His) c.335A>C c.465A>C (p.Gln155His) c.455A>C n.447A>C c.455A>C (n.455A>C) | |
| 18 | g.52906165A>G | CA503999353 | DCC | c.534A>G (p.Gln178=) c.335A>G c.465A>G (p.Gln155=) c.455A>G n.447A>G c.455A>G (n.455A>G) | |
| 18 | g.52906165A>T | CA402513730 | DCC | c.534A>T (p.Gln178His) c.335A>T c.465A>T (p.Gln155His) c.455A>T n.447A>T c.455A>T (n.455A>T) | |
| 18 | g.52906166G>A | CA402513731 | DCC | c.535G>A (p.Asp179Asn) c.336G>A c.466G>A (p.Asp156Asn) c.456G>A n.448G>A c.456G>A (n.456G>A) | gnomAD v4 |
| 18 | g.52906166G>C | CA402513732 | DCC | c.535G>C (p.Asp179His) c.336G>C c.466G>C (p.Asp156His) c.456G>C n.448G>C c.456G>C (n.456G>C) | |
| 18 | g.52906166G>T | CA402513733 | DCC | c.535G>T (p.Asp179Tyr) c.336G>T c.466G>T (p.Asp156Tyr) c.456G>T n.448G>T c.456G>T (n.456G>T) | |
| 18 | g.52906167A>C | CA402513734 | DCC | c.536A>C (p.Asp179Ala) c.337A>C c.467A>C (p.Asp156Ala) c.457A>C n.449A>C c.457A>C (n.457A>C) | |
| 18 | g.52906167A>G | CA402513736 | DCC | c.536A>G (p.Asp179Gly) c.337A>G c.467A>G (p.Asp156Gly) c.457A>G n.449A>G c.457A>G (n.457A>G) | |
| 18 | g.52906167A>T | CA402513735 | DCC | c.536A>T (p.Asp179Val) c.337A>T c.467A>T (p.Asp156Val) c.457A>T n.449A>T c.457A>T (n.457A>T) | |
| 18 | g.52906168C>A | CA402513737 | DCC | c.537C>A (p.Asp179Glu) c.338C>A c.468C>A (p.Asp156Glu) c.458C>A n.450C>A c.458C>A (n.458C>A) | gnomAD v4 |
| 18 | g.52906168C>G | CA402513738 | DCC | c.537C>G (p.Asp179Glu) c.338C>G c.468C>G (p.Asp156Glu) c.458C>G n.450C>G c.458C>G (n.458C>G) | |
| 18 | g.52906168C>T | CA503999354 | DCC | c.537C>T (p.Asp179=) c.338C>T c.468C>T (p.Asp156=) c.458C>T n.450C>T c.458C>T (n.458C>T) | |
| 18 | g.52906169C>A | CA402513739 | DCC | c.538C>A (p.Leu180Met) c.339C>A c.469C>A (p.Leu157Met) c.459C>A n.451C>A c.459C>A (n.459C>A) | |
| 18 | g.52906169C>G | CA402513740 | DCC | c.538C>G (p.Leu180Val) c.339C>G c.469C>G (p.Leu157Val) c.459C>G n.451C>G c.459C>G (n.459C>G) | |
| 18 | g.52906169C>T | CA503999355 | DCC | c.538C>T (p.Leu180=) c.339C>T c.469C>T (p.Leu157=) c.459C>T n.451C>T c.459C>T (n.459C>T) | |
| 18 | g.52906170T>A | CA402513741 | DCC | c.539T>A (p.Leu180Gln) c.340T>A c.470T>A (p.Leu157Gln) c.460T>A n.452T>A c.460T>A (n.460T>A) | |
| 18 | g.52906170T>C | CA402513743 | DCC | c.539T>C (p.Leu180Pro) c.340T>C c.470T>C (p.Leu157Pro) c.460T>C n.452T>C c.460T>C (n.460T>C) | |
| 18 | g.52906170T>G | CA402513742 | DCC | c.539T>G (p.Leu180Arg) c.340T>G c.470T>G (p.Leu157Arg) c.460T>G n.452T>G c.460T>G (n.460T>G) | |
| 18 | g.52906171G>A | CA300657951 | DCC | c.540G>A (p.Leu180=) c.341G>A c.471G>A (p.Leu157=) c.461G>A n.453G>A c.461G>A (n.461G>A) | dbSNP gnomAD v4 |
| 18 | g.52906171G>C | CA503999357 | DCC | c.540G>C (p.Leu180=) c.341G>C c.471G>C (p.Leu157=) c.461G>C n.453G>C c.461G>C (n.461G>C) | |
| 18 | g.52906171G= | CA2303875048 | DCC | c.540G= (p.Leu180=) c.341G= c.471G= (p.Leu157=) c.461G= n.453G= c.461G= (n.461G=) | |
| 18 | g.52906171G>T | CA503999356 | DCC | c.540G>T (p.Leu180=) c.341G>T c.471G>T (p.Leu157=) c.461G>T n.453G>T c.461G>T (n.461G>T) |