Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55191847G>A | CA135949 | EGFR | c.2439G>A (p.Glu813=) c.899+48G>A c.2598G>A (p.Glu866=) c.*28+18919G>A (n.*28+18919G>A) c.2463G>A (p.Glu821=) c.1797G>A (p.Glu599=) | ClinVar dbSNP |
7 | g.55191847G>C | CA367580320 | EGFR | c.2439G>C (p.Glu813Asp) c.899+48G>C c.2598G>C (p.Glu866Asp) c.*28+18919G>C (n.*28+18919G>C) c.2463G>C (p.Glu821Asp) c.1797G>C (p.Glu599Asp) | dbSNP COSMIC |
7 | g.55191847G= | CA1708922700 | EGFR | c.2439G= (p.Glu813=) c.899+48G= c.2598G= (p.Glu866=) c.*28+18919G= (n.*28+18919G=) c.2463G= (p.Glu821=) c.1797G= (p.Glu599=) | |
7 | g.55191847G>T | CA367580321 | EGFR | c.2439G>T (p.Glu813Asp) c.899+48G>T c.2598G>T (p.Glu866Asp) c.*28+18919G>T (n.*28+18919G>T) c.2463G>T (p.Glu821Asp) c.1797G>T (p.Glu599Asp) | COSMIC |
7 | g.55191848A>C | CA367580322 | EGFR | c.2440A>C (p.Lys814Gln) c.899+49A>C c.2599A>C (p.Lys867Gln) c.*28+18920A>C (n.*28+18920A>C) c.2464A>C (p.Lys822Gln) c.1798A>C (p.Lys600Gln) | |
7 | g.55191848A>G | CA367580324 | EGFR | c.2440A>G (p.Lys814Glu) c.899+49A>G c.2599A>G (p.Lys867Glu) c.*28+18920A>G (n.*28+18920A>G) c.2464A>G (p.Lys822Glu) c.1798A>G (p.Lys600Glu) | dbSNP |
7 | g.55191848A>T | CA367580323 | EGFR | c.2440A>T (p.Lys814Ter) c.899+49A>T c.2599A>T (p.Lys867Ter) c.*28+18920A>T (n.*28+18920A>T) c.2464A>T (p.Lys822Ter) c.1798A>T (p.Lys600Ter) | |
7 | g.55191849A>C | CA367580325 | EGFR | c.2441A>C (p.Lys814Thr) c.899+50A>C c.2600A>C (p.Lys867Thr) c.*28+18921A>C (n.*28+18921A>C) c.2465A>C (p.Lys822Thr) c.1799A>C (p.Lys600Thr) | |
7 | g.55191849A>G | CA367580326 | EGFR | c.2441A>G (p.Lys814Arg) c.899+50A>G c.2600A>G (p.Lys867Arg) c.*28+18921A>G (n.*28+18921A>G) c.2465A>G (p.Lys822Arg) c.1799A>G (p.Lys600Arg) | dbSNP gnomAD v4 |
7 | g.55191849A>T | CA367580327 | EGFR | c.2441A>T (p.Lys814Ile) c.899+50A>T c.2600A>T (p.Lys867Ile) c.*28+18921A>T (n.*28+18921A>T) c.2465A>T (p.Lys822Ile) c.1799A>T (p.Lys600Ile) | |
7 | g.55191850A>C | CA367580328 | EGFR | c.2442A>C (p.Lys814Asn) c.899+51A>C c.2601A>C (p.Lys867Asn) c.*28+18922A>C (n.*28+18922A>C) c.2466A>C (p.Lys822Asn) c.1800A>C (p.Lys600Asn) | dbSNP |
7 | g.55191850A>G | CA454965667 | EGFR | c.2442A>G (p.Lys814=) c.899+51A>G c.2601A>G (p.Lys867=) c.*28+18922A>G (n.*28+18922A>G) c.2466A>G (p.Lys822=) c.1800A>G (p.Lys600=) | dbSNP |
7 | g.55191850A>T | CA367580329 | EGFR | c.2442A>T (p.Lys814Asn) c.899+51A>T c.2601A>T (p.Lys867Asn) c.*28+18922A>T (n.*28+18922A>T) c.2466A>T (p.Lys822Asn) c.1800A>T (p.Lys600Asn) | dbSNP |
7 | g.55191851G>A | CA269859 | EGFR | c.2443G>A (p.Glu815Lys) c.899+52G>A c.2602G>A (p.Glu868Lys) c.*28+18923G>A (n.*28+18923G>A) c.2467G>A (p.Glu823Lys) c.1801G>A (p.Glu601Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
7 | g.55191851G>C | CA367580330 | EGFR | c.2443G>C (p.Glu815Gln) c.899+52G>C c.2602G>C (p.Glu868Gln) c.*28+18923G>C (n.*28+18923G>C) c.2467G>C (p.Glu823Gln) c.1801G>C (p.Glu601Gln) | dbSNP gnomAD v2 |
7 | g.55191851G= | CA1708922712 | EGFR | c.2443G= (p.Glu815=) c.899+52G= c.2602G= (p.Glu868=) c.*28+18923G= (n.*28+18923G=) c.2467G= (p.Glu823=) c.1801G= (p.Glu601=) | |
7 | g.55191851G>T | CA367580331 | EGFR | c.2443G>T (p.Glu815Ter) c.899+52G>T c.2602G>T (p.Glu868Ter) c.*28+18923G>T (n.*28+18923G>T) c.2467G>T (p.Glu823Ter) c.1801G>T (p.Glu601Ter) | |
7 | g.55191852A>C | CA367580332 | EGFR | c.2444A>C (p.Glu815Ala) c.899+53A>C c.2603A>C (p.Glu868Ala) c.*28+18924A>C (n.*28+18924A>C) c.2468A>C (p.Glu823Ala) c.1802A>C (p.Glu601Ala) | |
7 | g.55191852A>G | CA367580333 | EGFR | c.2444A>G (p.Glu815Gly) c.899+53A>G c.2603A>G (p.Glu868Gly) c.*28+18924A>G (n.*28+18924A>G) c.2468A>G (p.Glu823Gly) c.1802A>G (p.Glu601Gly) | dbSNP COSMIC |
7 | g.55191852A>T | CA367580334 | EGFR | c.2444A>T (p.Glu815Val) c.899+53A>T c.2603A>T (p.Glu868Val) c.*28+18924A>T (n.*28+18924A>T) c.2468A>T (p.Glu823Val) c.1802A>T (p.Glu601Val) | dbSNP COSMIC |
7 | g.55191853A>C | CA367580336 | EGFR | c.2445A>C (p.Glu815Asp) c.899+54A>C c.2604A>C (p.Glu868Asp) c.*28+18925A>C (n.*28+18925A>C) c.2469A>C (p.Glu823Asp) c.1803A>C (p.Glu601Asp) | dbSNP |
7 | g.55191853A>G | CA454965668 | EGFR | c.2445A>G (p.Glu815=) c.899+54A>G c.2604A>G (p.Glu868=) c.*28+18925A>G (n.*28+18925A>G) c.2469A>G (p.Glu823=) c.1803A>G (p.Glu601=) | ClinVar dbSNP gnomAD v4 |
7 | g.55191853A>T | CA367580335 | EGFR | c.2445A>T (p.Glu815Asp) c.899+54A>T c.2604A>T (p.Glu868Asp) c.*28+18925A>T (n.*28+18925A>T) c.2469A>T (p.Glu823Asp) c.1803A>T (p.Glu601Asp) | COSMIC |
7 | g.55191854T>A | CA367580337 | EGFR | c.2446T>A (p.Tyr816Asn) c.899+55T>A c.2605T>A (p.Tyr869Asn) c.*28+18926T>A (n.*28+18926T>A) c.2470T>A (p.Tyr824Asn) c.1804T>A (p.Tyr602Asn) | dbSNP |
7 | g.55191854T>C | CA367580338 | EGFR | c.2446T>C (p.Tyr816His) c.899+55T>C c.2605T>C (p.Tyr869His) c.*28+18926T>C (n.*28+18926T>C) c.2470T>C (p.Tyr824His) c.1804T>C (p.Tyr602His) | ClinVar |
7 | g.55191854T>G | CA367580339 | EGFR | c.2446T>G (p.Tyr816Asp) c.899+55T>G c.2605T>G (p.Tyr869Asp) c.*28+18926T>G (n.*28+18926T>G) c.2470T>G (p.Tyr824Asp) c.1804T>G (p.Tyr602Asp) | |
7 | g.55191855A= | CA1708922717 | EGFR | c.2447A= (p.Tyr816=) c.899+56A= c.2606A= (p.Tyr869=) c.*28+18927A= (n.*28+18927A=) c.2471A= (p.Tyr824=) c.1805A= (p.Tyr602=) | |
7 | g.55191855A>C | CA367580340 | EGFR | c.2447A>C (p.Tyr816Ser) c.899+56A>C c.2606A>C (p.Tyr869Ser) c.*28+18927A>C (n.*28+18927A>C) c.2471A>C (p.Tyr824Ser) c.1805A>C (p.Tyr602Ser) | |
7 | g.55191855A>G | CA367580341 | EGFR | c.2447A>G (p.Tyr816Cys) c.899+56A>G c.2606A>G (p.Tyr869Cys) c.*28+18927A>G (n.*28+18927A>G) c.2471A>G (p.Tyr824Cys) c.1805A>G (p.Tyr602Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55191855A>T | CA367580342 | EGFR | c.2447A>T (p.Tyr816Phe) c.899+56A>T c.2606A>T (p.Tyr869Phe) c.*28+18927A>T (n.*28+18927A>T) c.2471A>T (p.Tyr824Phe) c.1805A>T (p.Tyr602Phe) | |
7 | g.55191856C>A | CA367580343 | EGFR | c.2448C>A (p.Tyr816Ter) c.899+57C>A c.2607C>A (p.Tyr869Ter) c.*28+18928C>A (n.*28+18928C>A) c.2472C>A (p.Tyr824Ter) c.1806C>A (p.Tyr602Ter) | |
7 | g.55191856C>G | CA367580344 | EGFR | c.2448C>G (p.Tyr816Ter) c.899+57C>G c.2607C>G (p.Tyr869Ter) c.*28+18928C>G (n.*28+18928C>G) c.2472C>G (p.Tyr824Ter) c.1806C>G (p.Tyr602Ter) | |
7 | g.55191856C>T | CA454965669 | EGFR | c.2448C>T (p.Tyr816=) c.899+57C>T c.2607C>T (p.Tyr869=) c.*28+18928C>T (n.*28+18928C>T) c.2472C>T (p.Tyr824=) c.1806C>T (p.Tyr602=) | ClinVar dbSNP |
7 | g.55191857C>A | CA367580345 | EGFR | c.2449C>A (p.His817Asn) c.899+58C>A c.2608C>A (p.His870Asn) c.*28+18929C>A (n.*28+18929C>A) c.2473C>A (p.His825Asn) c.1807C>A (p.His603Asn) | dbSNP |
7 | g.55191857C>G | CA367580346 | EGFR | c.2449C>G (p.His817Asp) c.899+58C>G c.2608C>G (p.His870Asp) c.*28+18929C>G (n.*28+18929C>G) c.2473C>G (p.His825Asp) c.1807C>G (p.His603Asp) | dbSNP |
7 | g.55191857C>T | CA367580347 | EGFR | c.2449C>T (p.His817Tyr) c.899+58C>T c.2608C>T (p.His870Tyr) c.*28+18929C>T (n.*28+18929C>T) c.2473C>T (p.His825Tyr) c.1807C>T (p.His603Tyr) | dbSNP COSMIC |
7 | g.55191858A= | CA1708922720 | EGFR | c.2450A= (p.His817=) c.899+59A= c.2609A= (p.His870=) c.*28+18930A= (n.*28+18930A=) c.2474A= (p.His825=) c.1808A= (p.His603=) | |
7 | g.55191858A>C | CA367580348 | EGFR | c.2450A>C (p.His817Pro) c.899+59A>C c.2609A>C (p.His870Pro) c.*28+18930A>C (n.*28+18930A>C) c.2474A>C (p.His825Pro) c.1808A>C (p.His603Pro) | dbSNP |
7 | g.55191858A>G | CA367580349 | EGFR | c.2450A>G (p.His817Arg) c.899+59A>G c.2609A>G (p.His870Arg) c.*28+18930A>G (n.*28+18930A>G) c.2474A>G (p.His825Arg) c.1808A>G (p.His603Arg) | ClinVar dbSNP COSMIC |
7 | g.55191858A>T | CA367580350 | EGFR | c.2450A>T (p.His817Leu) c.899+59A>T c.2609A>T (p.His870Leu) c.*28+18930A>T (n.*28+18930A>T) c.2474A>T (p.His825Leu) c.1808A>T (p.His603Leu) | dbSNP |
7 | g.55191859T>A | CA367580352 | EGFR | c.2451T>A (p.His817Gln) c.899+60T>A c.2610T>A (p.His870Gln) c.*28+18931T>A (n.*28+18931T>A) c.2475T>A (p.His825Gln) c.1809T>A (p.His603Gln) | |
7 | g.55191859T>C | CA454965670 | EGFR | c.2451T>C (p.His817=) c.899+60T>C c.2610T>C (p.His870=) c.*28+18931T>C (n.*28+18931T>C) c.2475T>C (p.His825=) c.1809T>C (p.His603=) | ClinVar dbSNP gnomAD v4 |
7 | g.55191859T>G | CA367580351 | EGFR | c.2451T>G (p.His817Gln) c.899+60T>G c.2610T>G (p.His870Gln) c.*28+18931T>G (n.*28+18931T>G) c.2475T>G (p.His825Gln) c.1809T>G (p.His603Gln) | |
7 | g.55191859T= | CA1708922723 | EGFR | c.2451T= (p.His817=) c.899+60T= c.2610T= (p.His870=) c.*28+18931T= (n.*28+18931T=) c.2475T= (p.His825=) c.1809T= (p.His603=) | |
7 | g.55191860G>A | CA367580353 | EGFR | c.2452G>A (p.Ala818Thr) c.899+61G>A c.2611G>A (p.Ala871Thr) c.*28+18932G>A (n.*28+18932G>A) c.2476G>A (p.Ala826Thr) c.1810G>A (p.Ala604Thr) | dbSNP COSMIC |
7 | g.55191860G>C | CA367580354 | EGFR | c.2452G>C (p.Ala818Pro) c.899+61G>C c.2611G>C (p.Ala871Pro) c.*28+18932G>C (n.*28+18932G>C) c.2476G>C (p.Ala826Pro) c.1810G>C (p.Ala604Pro) | dbSNP |
7 | g.55191860G>T | CA367580355 | EGFR | c.2452G>T (p.Ala818Ser) c.899+61G>T c.2611G>T (p.Ala871Ser) c.*28+18932G>T (n.*28+18932G>T) c.2476G>T (p.Ala826Ser) c.1810G>T (p.Ala604Ser) | |
7 | g.55191861C>A | CA367580356 | EGFR | c.2453C>A (p.Ala818Glu) c.899+62C>A c.2612C>A (p.Ala871Glu) c.*28+18933C>A (n.*28+18933C>A) c.2477C>A (p.Ala826Glu) c.1811C>A (p.Ala604Glu) | dbSNP |
7 | g.55191861C= | CA1708922729 | EGFR | c.2453C= (p.Ala818=) c.899+62C= c.2612C= (p.Ala871=) c.*28+18933C= (n.*28+18933C=) c.2477C= (p.Ala826=) c.1811C= (p.Ala604=) | |
7 | g.55191861C>G | CA135952 | EGFR | c.2453C>G (p.Ala818Gly) c.899+62C>G c.2612C>G (p.Ala871Gly) c.*28+18933C>G (n.*28+18933C>G) c.2477C>G (p.Ala826Gly) c.1811C>G (p.Ala604Gly) | ClinVar dbSNP COSMIC |