| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191724G>A | CA367580071 | EGFR | c.2475G>A (p.Met825Ile) c.*28+18796G>A (n.*28+18796G>A) c.2340G>A (p.Met780Ile) c.2316G>A (p.Met772Ile) c.1674G>A (p.Met558Ile) | COSMIC |
| 7 | g.55191724G>C | CA367580072 | EGFR | c.2475G>C (p.Met825Ile) c.*28+18796G>C (n.*28+18796G>C) c.2340G>C (p.Met780Ile) c.2316G>C (p.Met772Ile) c.1674G>C (p.Met558Ile) | |
| 7 | g.55191724G= | CA1708922388 | EGFR | c.2475G= (p.Met825=) c.*28+18796G= (n.*28+18796G=) c.2340G= (p.Met780=) c.2316G= (p.Met772=) c.1674G= (p.Met558=) | |
| 7 | g.55191724G>T | CA367580073 | EGFR | c.2475G>T (p.Met825Ile) c.*28+18796G>T (n.*28+18796G>T) c.2340G>T (p.Met780Ile) c.2316G>T (p.Met772Ile) c.1674G>T (p.Met558Ile) | ClinVar COSMIC |
| 7 | g.55191725A>C | CA367580074 | EGFR | c.2476A>C (p.Asn826His) c.*28+18797A>C (n.*28+18797A>C) c.2341A>C (p.Asn781His) c.2317A>C (p.Asn773His) c.1675A>C (p.Asn559His) | |
| 7 | g.55191725A>G | CA367580075 | EGFR | c.2476A>G (p.Asn826Asp) c.*28+18797A>G (n.*28+18797A>G) c.2341A>G (p.Asn781Asp) c.2317A>G (p.Asn773Asp) c.1675A>G (p.Asn559Asp) | |
| 7 | g.55191725A>T | CA367580076 | EGFR | c.2476A>T (p.Asn826Tyr) c.*28+18797A>T (n.*28+18797A>T) c.2341A>T (p.Asn781Tyr) c.2317A>T (p.Asn773Tyr) c.1675A>T (p.Asn559Tyr) | |
| 7 | g.55191726A>C | CA367580079 | EGFR | c.2477A>C (p.Asn826Thr) c.*28+18798A>C (n.*28+18798A>C) c.2342A>C (p.Asn781Thr) c.2318A>C (p.Asn773Thr) c.1676A>C (p.Asn559Thr) | |
| 7 | g.55191726A>G | CA367580077 | EGFR | c.2477A>G (p.Asn826Ser) c.*28+18798A>G (n.*28+18798A>G) c.2342A>G (p.Asn781Ser) c.2318A>G (p.Asn773Ser) c.1676A>G (p.Asn559Ser) | COSMIC |
| 7 | g.55191726A>T | CA367580078 | EGFR | c.2477A>T (p.Asn826Ile) c.*28+18798A>T (n.*28+18798A>T) c.2342A>T (p.Asn781Ile) c.2318A>T (p.Asn773Ile) c.1676A>T (p.Asn559Ile) | |
| 7 | g.55191727C>A | CA367580080 | EGFR | c.2478C>A (p.Asn826Lys) c.*28+18799C>A (n.*28+18799C>A) c.2343C>A (p.Asn781Lys) c.2319C>A (p.Asn773Lys) c.1677C>A (p.Asn559Lys) | |
| 7 | g.55191727C>G | CA367580081 | EGFR | c.2478C>G (p.Asn826Lys) c.*28+18799C>G (n.*28+18799C>G) c.2343C>G (p.Asn781Lys) c.2319C>G (p.Asn773Lys) c.1677C>G (p.Asn559Lys) | |
| 7 | g.55191727C>T | CA454965576 | EGFR | c.2478C>T (p.Asn826=) c.*28+18799C>T (n.*28+18799C>T) c.2343C>T (p.Asn781=) c.2319C>T (p.Asn773=) c.1677C>T (p.Asn559=) | |
| 7 | g.55191728T>A | CA367580082 | EGFR | c.2479T>A (p.Tyr827Asn) c.*28+18800T>A (n.*28+18800T>A) c.2344T>A (p.Tyr782Asn) c.2320T>A (p.Tyr774Asn) c.1678T>A (p.Tyr560Asn) | |
| 7 | g.55191728T>C | CA367580083 | EGFR | c.2479T>C (p.Tyr827His) c.*28+18800T>C (n.*28+18800T>C) c.2344T>C (p.Tyr782His) c.2320T>C (p.Tyr774His) c.1678T>C (p.Tyr560His) | |
| 7 | g.55191728T>G | CA367580084 | EGFR | c.2479T>G (p.Tyr827Asp) c.*28+18800T>G (n.*28+18800T>G) c.2344T>G (p.Tyr782Asp) c.2320T>G (p.Tyr774Asp) c.1678T>G (p.Tyr560Asp) | |
| 7 | g.55191728T= | CA1708922393 | EGFR | c.2479T= (p.Tyr827=) c.*28+18800T= (n.*28+18800T=) c.2344T= (p.Tyr782=) c.2320T= (p.Tyr774=) c.1678T= (p.Tyr560=) | |
| 7 | g.55191729A= | CA1708922398 | EGFR | c.2480A= (p.Tyr827=) c.*28+18801A= (n.*28+18801A=) c.2345A= (p.Tyr782=) c.2321A= (p.Tyr774=) c.1679A= (p.Tyr560=) | |
| 7 | g.55191729A>C | CA367580085 | EGFR | c.2480A>C (p.Tyr827Ser) c.*28+18801A>C (n.*28+18801A>C) c.2345A>C (p.Tyr782Ser) c.2321A>C (p.Tyr774Ser) c.1679A>C (p.Tyr560Ser) | |
| 7 | g.55191729A>G | CA367580086 | EGFR | c.2480A>G (p.Tyr827Cys) c.*28+18801A>G (n.*28+18801A>G) c.2345A>G (p.Tyr782Cys) c.2321A>G (p.Tyr774Cys) c.1679A>G (p.Tyr560Cys) | |
| 7 | g.55191729A>T | CA158934114 | EGFR | c.2480A>T (p.Tyr827Phe) c.*28+18801A>T (n.*28+18801A>T) c.2345A>T (p.Tyr782Phe) c.2321A>T (p.Tyr774Phe) c.1679A>T (p.Tyr560Phe) | ClinVar dbSNP |
| 7 | g.55191730C>A | CA367580087 | EGFR | c.2481C>A (p.Tyr827Ter) c.*28+18802C>A (n.*28+18802C>A) c.2346C>A (p.Tyr782Ter) c.2322C>A (p.Tyr774Ter) c.1680C>A (p.Tyr560Ter) | COSMIC |
| 7 | g.55191730C>G | CA367580088 | EGFR | c.2481C>G (p.Tyr827Ter) c.*28+18802C>G (n.*28+18802C>G) c.2346C>G (p.Tyr782Ter) c.2322C>G (p.Tyr774Ter) c.1680C>G (p.Tyr560Ter) | |
| 7 | g.55191730C>T | CA454965578 | EGFR | c.2481C>T (p.Tyr827=) c.*28+18802C>T (n.*28+18802C>T) c.2346C>T (p.Tyr782=) c.2322C>T (p.Tyr774=) c.1680C>T (p.Tyr560=) | COSMIC |
| 7 | g.55191731T>A | CA367580089 | EGFR | c.2482T>A (p.Leu828Met) c.*28+18803T>A (n.*28+18803T>A) c.2347T>A (p.Leu783Met) c.2323T>A (p.Leu775Met) c.1681T>A (p.Leu561Met) | |
| 7 | g.55191731T>C | CA454965579 | EGFR | c.2482T>C (p.Leu828=) c.*28+18803T>C (n.*28+18803T>C) c.2347T>C (p.Leu783=) c.2323T>C (p.Leu775=) c.1681T>C (p.Leu561=) | |
| 7 | g.55191731T>G | CA367580090 | EGFR | c.2482T>G (p.Leu828Val) c.*28+18803T>G (n.*28+18803T>G) c.2347T>G (p.Leu783Val) c.2323T>G (p.Leu775Val) c.1681T>G (p.Leu561Val) | |
| 7 | g.55191732T>A | CA367580092 | EGFR | c.2483T>A (p.Leu828Ter) c.*28+18804T>A (n.*28+18804T>A) c.2348T>A (p.Leu783Ter) c.2324T>A (p.Leu775Ter) c.1682T>A (p.Leu561Ter) | COSMIC |
| 7 | g.55191732T>C | CA367580093 | EGFR | c.2483T>C (p.Leu828Ser) c.*28+18804T>C (n.*28+18804T>C) c.2348T>C (p.Leu783Ser) c.2324T>C (p.Leu775Ser) c.1682T>C (p.Leu561Ser) | |
| 7 | g.55191732T>G | CA367580091 | EGFR | c.2483T>G (p.Leu828Trp) c.*28+18804T>G (n.*28+18804T>G) c.2348T>G (p.Leu783Trp) c.2324T>G (p.Leu775Trp) c.1682T>G (p.Leu561Trp) | |
| 7 | g.55191733G>A | CA180716 | EGFR | c.2484G>A (p.Leu828=) c.*28+18805G>A (n.*28+18805G>A) c.2349G>A (p.Leu783=) c.2325G>A (p.Leu775=) c.1683G>A (p.Leu561=) | ClinVar dbSNP ExAC gnomAD COSMIC |
| 7 | g.55191733G>C | CA367580094 | EGFR | c.2484G>C (p.Leu828Phe) c.*28+18805G>C (n.*28+18805G>C) c.2349G>C (p.Leu783Phe) c.2325G>C (p.Leu775Phe) c.1683G>C (p.Leu561Phe) | |
| 7 | g.55191733G= | CA1708922405 | EGFR | c.2484G= (p.Leu828=) c.*28+18805G= (n.*28+18805G=) c.2349G= (p.Leu783=) c.2325G= (p.Leu775=) c.1683G= (p.Leu561=) | |
| 7 | g.55191733G>T | CA367580095 | EGFR | c.2484G>T (p.Leu828Phe) c.*28+18805G>T (n.*28+18805G>T) c.2349G>T (p.Leu783Phe) c.2325G>T (p.Leu775Phe) c.1683G>T (p.Leu561Phe) | |
| 7 | g.55191734G>A | CA367580096 | EGFR | c.2485G>A (p.Glu829Lys) c.*28+18806G>A (n.*28+18806G>A) c.2350G>A (p.Glu784Lys) c.2326G>A (p.Glu776Lys) c.1684G>A (p.Glu562Lys) | COSMIC |
| 7 | g.55191734G>C | CA367580097 | EGFR | c.2485G>C (p.Glu829Gln) c.*28+18806G>C (n.*28+18806G>C) c.2350G>C (p.Glu784Gln) c.2326G>C (p.Glu776Gln) c.1684G>C (p.Glu562Gln) | ClinVar |
| 7 | g.55191734G= | CA1708922413 | EGFR | c.2485G= (p.Glu829=) c.*28+18806G= (n.*28+18806G=) c.2350G= (p.Glu784=) c.2326G= (p.Glu776=) c.1684G= (p.Glu562=) | |
| 7 | g.55191734G>T | CA367580098 | EGFR | c.2485G>T (p.Glu829Ter) c.*28+18806G>T (n.*28+18806G>T) c.2350G>T (p.Glu784Ter) c.2326G>T (p.Glu776Ter) c.1684G>T (p.Glu562Ter) | |
| 7 | g.55191735A>C | CA367580101 | EGFR | c.2486A>C (p.Glu829Ala) c.*28+18807A>C (n.*28+18807A>C) c.2351A>C (p.Glu784Ala) c.2327A>C (p.Glu776Ala) c.1685A>C (p.Glu562Ala) | |
| 7 | g.55191735A>G | CA367580100 | EGFR | c.2486A>G (p.Glu829Gly) c.*28+18807A>G (n.*28+18807A>G) c.2351A>G (p.Glu784Gly) c.2327A>G (p.Glu776Gly) c.1685A>G (p.Glu562Gly) | |
| 7 | g.55191735A>T | CA367580099 | EGFR | c.2486A>T (p.Glu829Val) c.*28+18807A>T (n.*28+18807A>T) c.2351A>T (p.Glu784Val) c.2327A>T (p.Glu776Val) c.1685A>T (p.Glu562Val) | |
| 7 | g.55191736G>A | CA4266101 | EGFR | c.2487G>A (p.Glu829=) c.*28+18808G>A (n.*28+18808G>A) c.2352G>A (p.Glu784=) c.2328G>A (p.Glu776=) c.1686G>A (p.Glu562=) | ClinVar dbSNP ExAC gnomAD COSMIC |
| 7 | g.55191736G>C | CA367580102 | EGFR | c.2487G>C (p.Glu829Asp) c.*28+18808G>C (n.*28+18808G>C) c.2352G>C (p.Glu784Asp) c.2328G>C (p.Glu776Asp) c.1686G>C (p.Glu562Asp) | |
| 7 | g.55191736G= | CA1708922418 | EGFR | c.2487G= (p.Glu829=) c.*28+18808G= (n.*28+18808G=) c.2352G= (p.Glu784=) c.2328G= (p.Glu776=) c.1686G= (p.Glu562=) | |
| 7 | g.55191736G>T | CA367580103 | EGFR | c.2487G>T (p.Glu829Asp) c.*28+18808G>T (n.*28+18808G>T) c.2352G>T (p.Glu784Asp) c.2328G>T (p.Glu776Asp) c.1686G>T (p.Glu562Asp) | |
| 7 | g.55191737G>A | CA367580104 | EGFR | c.2488G>A (p.Asp830Asn) c.*28+18809G>A (n.*28+18809G>A) c.2353G>A (p.Asp785Asn) c.2329G>A (p.Asp777Asn) c.1687G>A (p.Asp563Asn) | |
| 7 | g.55191737G>C | CA367580105 | EGFR | c.2488G>C (p.Asp830His) c.*28+18809G>C (n.*28+18809G>C) c.2353G>C (p.Asp785His) c.2329G>C (p.Asp777His) c.1687G>C (p.Asp563His) | |
| 7 | g.55191737G>T | CA367580106 | EGFR | c.2488G>T (p.Asp830Tyr) c.*28+18809G>T (n.*28+18809G>T) c.2353G>T (p.Asp785Tyr) c.2329G>T (p.Asp777Tyr) c.1687G>T (p.Asp563Tyr) | |
| 7 | g.55191738A>C | CA367580109 | EGFR | c.2489A>C (p.Asp830Ala) c.*28+18810A>C (n.*28+18810A>C) c.2354A>C (p.Asp785Ala) c.2330A>C (p.Asp777Ala) c.1688A>C (p.Asp563Ala) | |
| 7 | g.55191738A>G | CA367580107 | EGFR | c.2489A>G (p.Asp830Gly) c.*28+18810A>G (n.*28+18810A>G) c.2354A>G (p.Asp785Gly) c.2330A>G (p.Asp777Gly) c.1688A>G (p.Asp563Gly) |