| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738379G>A | CA372279484 | MYC | c.117G>A (p.Glu39=) c.159G>A (p.Glu53=) c.162G>A (p.Glu54=) c.-184G>A (n.-184G>A) c.83G>A (p.Ser28Asn) | dbSNP COSMIC COSMIC |
| 8 | g.127738379G>C | CA122524 | MYC | c.117G>C (p.Glu39Asp) c.159G>C (p.Glu53Asp) c.162G>C (p.Glu54Asp) c.-184G>C (n.-184G>C) c.83G>C (p.Ser28Thr) | ClinVar dbSNP COSMIC COSMIC |
| 8 | g.127738379G= | CA1818466341 | MYC | c.117G= (p.Glu39=) c.159G= (p.Glu53=) c.162G= (p.Glu54=) c.-184G= (n.-184G=) c.83G= (p.Ser28=) | |
| 8 | g.127738379G>T | CA372279483 | MYC | c.117G>T (p.Glu39Asp) c.159G>T (p.Glu53Asp) c.162G>T (p.Glu54Asp) c.-184G>T (n.-184G>T) c.83G>T (p.Ser28Ile) | COSMIC COSMIC |
| 8 | g.127738380C>A | CA372279485 | MYC | c.118C>A (p.Leu40Met) c.160C>A (p.Leu54Met) c.163C>A (p.Leu55Met) c.-183C>A (n.-183C>A) c.84C>A (p.Ser28Arg) | dbSNP COSMIC COSMIC |
| 8 | g.127738380C= | CA1818466348 | MYC | c.118C= (p.Leu40=) c.160C= (p.Leu54=) c.163C= (p.Leu55=) c.-183C= (n.-183C=) c.84C= (p.Ser28=) | |
| 8 | g.127738380C>G | CA372279486 | MYC | c.118C>G (p.Leu40Val) c.160C>G (p.Leu54Val) c.163C>G (p.Leu55Val) c.-183C>G (n.-183C>G) c.84C>G (p.Ser28Arg) | gnomAD v4 |
| 8 | g.127738380C>T | CA4875240 | MYC | c.118C>T (p.Leu40=) c.160C>T (p.Leu54=) c.163C>T (p.Leu55=) c.-183C>T (n.-183C>T) c.84C>T (p.Ser28=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738381T>A | CA372279487 | MYC | c.119T>A (p.Leu40Gln) c.161T>A (p.Leu54Gln) c.164T>A (p.Leu55Gln) c.-182T>A (n.-182T>A) c.85T>A (p.Cys29Ser) | dbSNP |
| 8 | g.127738381T>C | CA372279488 | MYC | c.119T>C (p.Leu40Pro) c.161T>C (p.Leu54Pro) c.164T>C (p.Leu55Pro) c.-182T>C (n.-182T>C) c.85T>C (p.Cys29Arg) | dbSNP gnomAD v2 |
| 8 | g.127738381T>G | CA372279489 | MYC | c.119T>G (p.Leu40Arg) c.161T>G (p.Leu54Arg) c.164T>G (p.Leu55Arg) c.-182T>G (n.-182T>G) c.85T>G (p.Cys29Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738381T= | CA1818466352 | MYC | c.119T= (p.Leu40=) c.161T= (p.Leu54=) c.164T= (p.Leu55=) c.-182T= (n.-182T=) c.85T= (p.Cys29=) | |
| 8 | g.127738382G>A | CA372279491 | MYC | c.120G>A (p.Leu40=) c.162G>A (p.Leu54=) c.165G>A (p.Leu55=) c.-181G>A (n.-181G>A) c.86G>A (p.Cys29Tyr) | dbSNP gnomAD v4 |
| 8 | g.127738382G>C | CA372279490 | MYC | c.120G>C (p.Leu40=) c.162G>C (p.Leu54=) c.165G>C (p.Leu55=) c.-181G>C (n.-181G>C) c.86G>C (p.Cys29Ser) | dbSNP |
| 8 | g.127738382G= | CA1818466355 | MYC | c.120G= (p.Leu40=) c.162G= (p.Leu54=) c.165G= (p.Leu55=) c.-181G= (n.-181G=) c.86G= (p.Cys29=) | |
| 8 | g.127738382G>T | CA4875241 | MYC | c.120G>T (p.Leu40=) c.162G>T (p.Leu54=) c.165G>T (p.Leu55=) c.-181G>T (n.-181G>T) c.86G>T (p.Cys29Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738383C>A | CA372279492 | MYC | c.121C>A (p.Gln41Lys) c.163C>A (p.Gln55Lys) c.166C>A (p.Gln56Lys) c.-180C>A (n.-180C>A) c.87C>A (p.Cys29Ter) | |
| 8 | g.127738383C>G | CA372279493 | MYC | c.121C>G (p.Gln41Glu) c.163C>G (p.Gln55Glu) c.166C>G (p.Gln56Glu) c.-180C>G (n.-180C>G) c.87C>G (p.Cys29Trp) | dbSNP |
| 8 | g.127738383C>T | CA372279494 | MYC | c.121C>T (p.Gln41Ter) c.163C>T (p.Gln55Ter) c.166C>T (p.Gln56Ter) c.-180C>T (n.-180C>T) c.87C>T (p.Cys29=) | dbSNP |
| 8 | g.127738384A>C | CA372279495 | MYC | c.122A>C (p.Gln41Pro) c.164A>C (p.Gln55Pro) c.167A>C (p.Gln56Pro) c.-179A>C (n.-179A>C) c.88A>C (p.Ser30Arg) | dbSNP |
| 8 | g.127738384A>G | CA372279496 | MYC | c.122A>G (p.Gln41Arg) c.164A>G (p.Gln55Arg) c.167A>G (p.Gln56Arg) c.-179A>G (n.-179A>G) c.88A>G (p.Ser30Gly) | dbSNP |
| 8 | g.127738384A>T | CA372279497 | MYC | c.122A>T (p.Gln41Leu) c.164A>T (p.Gln55Leu) c.167A>T (p.Gln56Leu) c.-179A>T (n.-179A>T) c.88A>T (p.Ser30Cys) | dbSNP |
| 8 | g.127738385G>A | CA372279498 | MYC | c.123G>A (p.Gln41=) c.165G>A (p.Gln55=) c.168G>A (p.Gln56=) c.-178G>A (n.-178G>A) c.89G>A (p.Ser30Asn) | gnomAD v4 |
| 8 | g.127738385G>C | CA372279500 | MYC | c.123G>C (p.Gln41His) c.165G>C (p.Gln55His) c.168G>C (p.Gln56His) c.-178G>C (n.-178G>C) c.89G>C (p.Ser30Thr) | dbSNP |
| 8 | g.127738385G>T | CA372279499 | MYC | c.123G>T (p.Gln41His) c.165G>T (p.Gln55His) c.168G>T (p.Gln56His) c.-178G>T (n.-178G>T) c.89G>T (p.Ser30Ile) | |
| 8 | g.127738386C>A | CA372279501 | MYC | c.124C>A (p.Pro42Thr) c.166C>A (p.Pro56Thr) c.169C>A (p.Pro57Thr) c.-177C>A (n.-177C>A) c.90C>A (p.Ser30Arg) | gnomAD v4 |
| 8 | g.127738386C= | CA1818466365 | MYC | c.124C= (p.Pro42=) c.166C= (p.Pro56=) c.169C= (p.Pro57=) c.-177C= (n.-177C=) c.90C= (p.Ser30=) | |
| 8 | g.127738386C>G | CA372279502 | MYC | c.124C>G (p.Pro42Ala) c.166C>G (p.Pro56Ala) c.169C>G (p.Pro57Ala) c.-177C>G (n.-177C>G) c.90C>G (p.Ser30Arg) | dbSNP |
| 8 | g.127738386C>T | CA16602745 | MYC | c.124C>T (p.Pro42Ser) c.166C>T (p.Pro56Ser) c.169C>T (p.Pro57Ser) c.-177C>T (n.-177C>T) c.90C>T (p.Ser30=) | ClinVar dbSNP gnomAD v4 |
| 8 | g.127738390del | CA2688552186 | MYC | c.128del (p.Pro43ArgfsTer?) c.170del (p.Pro57ArgfsTer?) c.173del (p.Pro58ArgfsTer?) c.-173del (n.-173del) c.94del (p.Arg32GlyfsTer21) | gnomAD v4 |
| 8 | g.127738387C>A | CA372279503 | MYC | c.125C>A (p.Pro42His) c.167C>A (p.Pro56His) c.170C>A (p.Pro57His) c.-176C>A (n.-176C>A) c.91C>A (p.Pro31Thr) | dbSNP |
| 8 | g.127738387C= | CA1818466370 | MYC | c.125C= (p.Pro42=) c.167C= (p.Pro56=) c.170C= (p.Pro57=) c.-176C= (n.-176C=) c.91C= (p.Pro31=) | |
| 8 | g.127738387C>G | CA372279504 | MYC | c.125C>G (p.Pro42Arg) c.167C>G (p.Pro56Arg) c.170C>G (p.Pro57Arg) c.-176C>G (n.-176C>G) c.91C>G (p.Pro31Ala) | |
| 8 | g.127738387C>T | CA185777062 | MYC | c.125C>T (p.Pro42Leu) c.167C>T (p.Pro56Leu) c.170C>T (p.Pro57Leu) c.-176C>T (n.-176C>T) c.91C>T (p.Pro31Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.127738388C>A | CA372279505 | MYC | c.126C>A (p.Pro42=) c.168C>A (p.Pro56=) c.171C>A (p.Pro57=) c.-175C>A (n.-175C>A) c.92C>A (p.Pro31His) | |
| 8 | g.127738388C= | CA1818466374 | MYC | c.126C= (p.Pro42=) c.168C= (p.Pro56=) c.171C= (p.Pro57=) c.-175C= (n.-175C=) c.92C= (p.Pro31=) | |
| 8 | g.127738388C>G | CA372279506 | MYC | c.126C>G (p.Pro42=) c.168C>G (p.Pro56=) c.171C>G (p.Pro57=) c.-175C>G (n.-175C>G) c.92C>G (p.Pro31Arg) | |
| 8 | g.127738388C>T | CA4875242 | MYC | c.126C>T (p.Pro42=) c.168C>T (p.Pro56=) c.171C>T (p.Pro57=) c.-175C>T (n.-175C>T) c.92C>T (p.Pro31Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738389C>A | CA372279507 | MYC | c.127C>A (p.Pro43Thr) c.169C>A (p.Pro57Thr) c.172C>A (p.Pro58Thr) c.-174C>A (n.-174C>A) c.93C>A (p.Pro31=) | |
| 8 | g.127738389C>G | CA372279508 | MYC | c.127C>G (p.Pro43Ala) c.169C>G (p.Pro57Ala) c.172C>G (p.Pro58Ala) c.-174C>G (n.-174C>G) c.93C>G (p.Pro31=) | gnomAD v4 |
| 8 | g.127738389C>T | CA372279509 | MYC | c.127C>T (p.Pro43Ser) c.169C>T (p.Pro57Ser) c.172C>T (p.Pro58Ser) c.-174C>T (n.-174C>T) c.93C>T (p.Pro31=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738390C>A | CA372279510 | MYC | c.128C>A (p.Pro43Gln) c.170C>A (p.Pro57Gln) c.173C>A (p.Pro58Gln) c.-173C>A (n.-173C>A) c.94C>A (p.Arg32=) | |
| 8 | g.127738390C= | CA1818466379 | MYC | c.128C= (p.Pro43=) c.170C= (p.Pro57=) c.173C= (p.Pro58=) c.-173C= (n.-173C=) c.94C= (p.Arg32=) | |
| 8 | g.127738390C>G | CA372279511 | MYC | c.128C>G (p.Pro43Arg) c.170C>G (p.Pro57Arg) c.173C>G (p.Pro58Arg) c.-173C>G (n.-173C>G) c.94C>G (p.Arg32Gly) | dbSNP |
| 8 | g.127738390C>T | CA16602893 | MYC | c.128C>T (p.Pro43Leu) c.170C>T (p.Pro57Leu) c.173C>T (p.Pro58Leu) c.-173C>T (n.-173C>T) c.94C>T (p.Arg32Trp) | ClinVar dbSNP |
| 8 | g.127738391G>A | CA372279512 | MYC | c.129G>A (p.Pro43=) c.171G>A (p.Pro57=) c.174G>A (p.Pro58=) c.-172G>A (n.-172G>A) c.95G>A (p.Arg32Gln) | dbSNP |
| 8 | g.127738391G>C | CA372279513 | MYC | c.129G>C (p.Pro43=) c.171G>C (p.Pro57=) c.174G>C (p.Pro58=) c.-172G>C (n.-172G>C) c.95G>C (p.Arg32Pro) | dbSNP |
| 8 | g.127738391G>T | CA372279514 | MYC | c.129G>T (p.Pro43=) c.171G>T (p.Pro57=) c.174G>T (p.Pro58=) c.-172G>T (n.-172G>T) c.95G>T (p.Arg32Leu) | gnomAD v4 |
| 8 | g.127738392G>A | CA372279515 | MYC | c.130G>A (p.Ala44Thr) c.172G>A (p.Ala58Thr) c.175G>A (p.Ala59Thr) c.-171G>A (n.-171G>A) c.96G>A (p.Arg32=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738392G>C | CA372279516 | MYC | c.130G>C (p.Ala44Pro) c.172G>C (p.Ala58Pro) c.175G>C (p.Ala59Pro) c.-171G>C (n.-171G>C) c.96G>C (p.Arg32=) | dbSNP |