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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191736G>A | CA4266101 | EGFR | c.2328G>A (p.Glu776=) c.836G>A c.2487G>A (p.Glu829=) c.*28+18808G>A (n.*28+18808G>A) c.2352G>A (p.Glu784=) c.1686G>A (p.Glu562=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191736G>C | CA367580102 | EGFR | c.2328G>C (p.Glu776Asp) c.836G>C c.2487G>C (p.Glu829Asp) c.*28+18808G>C (n.*28+18808G>C) c.2352G>C (p.Glu784Asp) c.1686G>C (p.Glu562Asp) | dbSNP |
| 7 | g.55191736G= | CA1708922418 | EGFR | c.2328G= (p.Glu776=) c.836G= c.2487G= (p.Glu829=) c.*28+18808G= (n.*28+18808G=) c.2352G= (p.Glu784=) c.1686G= (p.Glu562=) | |
| 7 | g.55191736G>T | CA367580103 | EGFR | c.2328G>T (p.Glu776Asp) c.836G>T c.2487G>T (p.Glu829Asp) c.*28+18808G>T (n.*28+18808G>T) c.2352G>T (p.Glu784Asp) c.1686G>T (p.Glu562Asp) | |
| 7 | g.55191737G>A | CA367580104 | EGFR | c.2329G>A (p.Asp777Asn) c.837G>A c.2488G>A (p.Asp830Asn) c.*28+18809G>A (n.*28+18809G>A) c.2353G>A (p.Asp785Asn) c.1687G>A (p.Asp563Asn) | dbSNP |
| 7 | g.55191737G>C | CA367580105 | EGFR | c.2329G>C (p.Asp777His) c.837G>C c.2488G>C (p.Asp830His) c.*28+18809G>C (n.*28+18809G>C) c.2353G>C (p.Asp785His) c.1687G>C (p.Asp563His) | dbSNP |
| 7 | g.55191737G>T | CA367580106 | EGFR | c.2329G>T (p.Asp777Tyr) c.837G>T c.2488G>T (p.Asp830Tyr) c.*28+18809G>T (n.*28+18809G>T) c.2353G>T (p.Asp785Tyr) c.1687G>T (p.Asp563Tyr) | |
| 7 | g.55191738A>C | CA367580109 | EGFR | c.2330A>C (p.Asp777Ala) c.838A>C c.2489A>C (p.Asp830Ala) c.*28+18810A>C (n.*28+18810A>C) c.2354A>C (p.Asp785Ala) c.1688A>C (p.Asp563Ala) | dbSNP |
| 7 | g.55191738A>G | CA367580107 | EGFR | c.2330A>G (p.Asp777Gly) c.838A>G c.2489A>G (p.Asp830Gly) c.*28+18810A>G (n.*28+18810A>G) c.2354A>G (p.Asp785Gly) c.1688A>G (p.Asp563Gly) | dbSNP |
| 7 | g.55191738A>T | CA367580108 | EGFR | c.2330A>T (p.Asp777Val) c.838A>T c.2489A>T (p.Asp830Val) c.*28+18810A>T (n.*28+18810A>T) c.2354A>T (p.Asp785Val) c.1688A>T (p.Asp563Val) | dbSNP |
| 7 | g.55191739C>A | CA367580110 | EGFR | c.2331C>A (p.Asp777Glu) c.839C>A c.2490C>A (p.Asp830Glu) c.*28+18811C>A (n.*28+18811C>A) c.2355C>A (p.Asp785Glu) c.1689C>A (p.Asp563Glu) | dbSNP |
| 7 | g.55191739C>G | CA367580111 | EGFR | c.2331C>G (p.Asp777Glu) c.839C>G c.2490C>G (p.Asp830Glu) c.*28+18811C>G (n.*28+18811C>G) c.2355C>G (p.Asp785Glu) c.1689C>G (p.Asp563Glu) | dbSNP |
| 7 | g.55191739C>T | CA454965581 | EGFR | c.2331C>T (p.Asp777=) c.839C>T c.2490C>T (p.Asp830=) c.*28+18811C>T (n.*28+18811C>T) c.2355C>T (p.Asp785=) c.1689C>T (p.Asp563=) | ClinVar dbSNP |
| 7 | g.55191740C>A | CA367580112 | EGFR | c.2332C>A (p.Arg778Ser) c.840C>A c.2491C>A (p.Arg831Ser) c.*28+18812C>A (n.*28+18812C>A) c.2356C>A (p.Arg786Ser) c.1690C>A (p.Arg564Ser) | dbSNP |
| 7 | g.55191740C= | CA1708922424 | EGFR | c.2332C= (p.Arg778=) c.840C= c.2491C= (p.Arg831=) c.*28+18812C= (n.*28+18812C=) c.2356C= (p.Arg786=) c.1690C= (p.Arg564=) | |
| 7 | g.55191740C>G | CA367580113 | EGFR | c.2332C>G (p.Arg778Gly) c.840C>G c.2491C>G (p.Arg831Gly) c.*28+18812C>G (n.*28+18812C>G) c.2356C>G (p.Arg786Gly) c.1690C>G (p.Arg564Gly) | dbSNP |
| 7 | g.55191740C>T | CA135911 | EGFR | c.2332C>T (p.Arg778Cys) c.840C>T c.2491C>T (p.Arg831Cys) c.*28+18812C>T (n.*28+18812C>T) c.2356C>T (p.Arg786Cys) c.1690C>T (p.Arg564Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191741G>A | CA4266102 | EGFR | c.2333G>A (p.Arg778His) c.841G>A c.2492G>A (p.Arg831His) c.*28+18813G>A (n.*28+18813G>A) c.2357G>A (p.Arg786His) c.1691G>A (p.Arg564His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191741G>C | CA367580114 | EGFR | c.2333G>C (p.Arg778Pro) c.841G>C c.2492G>C (p.Arg831Pro) c.*28+18813G>C (n.*28+18813G>C) c.2357G>C (p.Arg786Pro) c.1691G>C (p.Arg564Pro) | dbSNP |
| 7 | g.55191741G= | CA1708922429 | EGFR | c.2333G= (p.Arg778=) c.841G= c.2492G= (p.Arg831=) c.*28+18813G= (n.*28+18813G=) c.2357G= (p.Arg786=) c.1691G= (p.Arg564=) | |
| 7 | g.55191741G>T | CA367580115 | EGFR | c.2333G>T (p.Arg778Leu) c.841G>T c.2492G>T (p.Arg831Leu) c.*28+18813G>T (n.*28+18813G>T) c.2357G>T (p.Arg786Leu) c.1691G>T (p.Arg564Leu) | dbSNP |
| 7 | g.55191742T>A | CA454965583 | EGFR | c.2334T>A (p.Arg778=) c.842T>A c.2493T>A (p.Arg831=) c.*28+18814T>A (n.*28+18814T>A) c.2358T>A (p.Arg786=) c.1692T>A (p.Arg564=) | dbSNP |
| 7 | g.55191742T>C | CA4266103 | EGFR | c.2334T>C (p.Arg778=) c.842T>C c.2493T>C (p.Arg831=) c.*28+18814T>C (n.*28+18814T>C) c.2358T>C (p.Arg786=) c.1692T>C (p.Arg564=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191742T>G | CA4266104 | EGFR | c.2334T>G (p.Arg778=) c.842T>G c.2493T>G (p.Arg831=) c.*28+18814T>G (n.*28+18814T>G) c.2358T>G (p.Arg786=) c.1692T>G (p.Arg564=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55191742T= | CA1708922434 | EGFR | c.2334T= (p.Arg778=) c.842T= c.2493T= (p.Arg831=) c.*28+18814T= (n.*28+18814T=) c.2358T= (p.Arg786=) c.1692T= (p.Arg564=) | |
| 7 | g.55191743C>A | CA367580116 | EGFR | c.2335C>A (p.Arg779Ser) c.843C>A c.2494C>A (p.Arg832Ser) c.*28+18815C>A (n.*28+18815C>A) c.2359C>A (p.Arg787Ser) c.1693C>A (p.Arg565Ser) | dbSNP |
| 7 | g.55191743C= | CA1708922439 | EGFR | c.2335C= (p.Arg779=) c.843C= c.2494C= (p.Arg832=) c.*28+18815C= (n.*28+18815C=) c.2359C= (p.Arg787=) c.1693C= (p.Arg565=) | |
| 7 | g.55191743C>G | CA367580117 | EGFR | c.2335C>G (p.Arg779Gly) c.843C>G c.2494C>G (p.Arg832Gly) c.*28+18815C>G (n.*28+18815C>G) c.2359C>G (p.Arg787Gly) c.1693C>G (p.Arg565Gly) | dbSNP |
| 7 | g.55191743C>T | CA4266105 | EGFR | c.2335C>T (p.Arg779Cys) c.843C>T c.2494C>T (p.Arg832Cys) c.*28+18815C>T (n.*28+18815C>T) c.2359C>T (p.Arg787Cys) c.1693C>T (p.Arg565Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191744G>A | CA4266106 | EGFR | c.2336G>A (p.Arg779His) c.844G>A c.2495G>A (p.Arg832His) c.*28+18816G>A (n.*28+18816G>A) c.2360G>A (p.Arg787His) c.1694G>A (p.Arg565His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191744G>C | CA367580119 | EGFR | c.2336G>C (p.Arg779Pro) c.844G>C c.2495G>C (p.Arg832Pro) c.*28+18816G>C (n.*28+18816G>C) c.2360G>C (p.Arg787Pro) c.1694G>C (p.Arg565Pro) | dbSNP gnomAD v4 |
| 7 | g.55191744G= | CA1708922443 | EGFR | c.2336G= (p.Arg779=) c.844G= c.2495G= (p.Arg832=) c.*28+18816G= (n.*28+18816G=) c.2360G= (p.Arg787=) c.1694G= (p.Arg565=) | |
| 7 | g.55191744G>T | CA367580118 | EGFR | c.2336G>T (p.Arg779Leu) c.844G>T c.2495G>T (p.Arg832Leu) c.*28+18816G>T (n.*28+18816G>T) c.2360G>T (p.Arg787Leu) c.1694G>T (p.Arg565Leu) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191745C>A | CA454965585 | EGFR | c.2337C>A (p.Arg779=) c.845C>A c.2496C>A (p.Arg832=) c.*28+18817C>A (n.*28+18817C>A) c.2361C>A (p.Arg787=) c.1695C>A (p.Arg565=) | dbSNP |
| 7 | g.55191745C>G | CA454965587 | EGFR | c.2337C>G (p.Arg779=) c.845C>G c.2496C>G (p.Arg832=) c.*28+18817C>G (n.*28+18817C>G) c.2361C>G (p.Arg787=) c.1695C>G (p.Arg565=) | dbSNP |
| 7 | g.55191745C>T | CA454965588 | EGFR | c.2337C>T (p.Arg779=) c.845C>T c.2496C>T (p.Arg832=) c.*28+18817C>T (n.*28+18817C>T) c.2361C>T (p.Arg787=) c.1695C>T (p.Arg565=) | ClinVar dbSNP |
| 7 | g.55191746T>A | CA367580120 | EGFR | c.2338T>A (p.Leu780Met) c.846T>A c.2497T>A (p.Leu833Met) c.*28+18818T>A (n.*28+18818T>A) c.2362T>A (p.Leu788Met) c.1696T>A (p.Leu566Met) | dbSNP |
| 7 | g.55191746T>C | CA454965589 | EGFR | c.2338T>C (p.Leu780=) c.846T>C c.2497T>C (p.Leu833=) c.*28+18818T>C (n.*28+18818T>C) c.2362T>C (p.Leu788=) c.1696T>C (p.Leu566=) | dbSNP |
| 7 | g.55191746T>G | CA135914 | EGFR | c.2338T>G (p.Leu780Val) c.846T>G c.2497T>G (p.Leu833Val) c.*28+18818T>G (n.*28+18818T>G) c.2362T>G (p.Leu788Val) c.1696T>G (p.Leu566Val) | ClinVar dbSNP COSMIC |
| 7 | g.55191746T= | CA1708922450 | EGFR | c.2338T= (p.Leu780=) c.846T= c.2497T= (p.Leu833=) c.*28+18818T= (n.*28+18818T=) c.2362T= (p.Leu788=) c.1696T= (p.Leu566=) | |
| 7 | g.55191746_55191747delinsCC | CA2573142232 | EGFR | c.2338_2339delinsCC (p.Leu780Pro) c.846_847delinsCC c.2497_2498delinsCC (p.Leu833Pro) c.*28+18818_*28+18819delinsCC (n.*28+18818_*28+18819delinsCC) c.2362_2363delinsCC (p.Leu788Pro) c.1696_1697delinsCC (p.Leu566Pro) | ClinVar dbSNP |
| 7 | g.55191747T>A | CA367580121 | EGFR | c.2339T>A (p.Leu780Ter) c.847T>A c.2498T>A (p.Leu833Ter) c.*28+18819T>A (n.*28+18819T>A) c.2363T>A (p.Leu788Ter) c.1697T>A (p.Leu566Ter) | dbSNP |
| 7 | g.55191747T>C | CA367580122 | EGFR | c.2339T>C (p.Leu780Ser) c.847T>C c.2498T>C (p.Leu833Ser) c.*28+18819T>C (n.*28+18819T>C) c.2363T>C (p.Leu788Ser) c.1697T>C (p.Leu566Ser) | |
| 7 | g.55191747T>G | CA367580123 | EGFR | c.2339T>G (p.Leu780Trp) c.847T>G c.2498T>G (p.Leu833Trp) c.*28+18819T>G (n.*28+18819T>G) c.2363T>G (p.Leu788Trp) c.1697T>G (p.Leu566Trp) | dbSNP COSMIC |
| 7 | g.55191747_55191748delinsTG | CA1708922456 | EGFR | c.2339_2340delinsTG (p.Leu780=) c.847_848delinsTG c.2498_2499delinsTG (p.Leu833=) c.*28+18819_*28+18820delinsTG (n.*28+18819_*28+18820delinsTG) c.2363_2364delinsTG (p.Leu788=) c.1697_1698delinsTG (p.Leu566=) | |
| 7 | g.55191747_55191835delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG | CA1708922454 | EGFR | c.2339_2427delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu780=) c.847_899+36delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG c.2498_2586delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu833=) c.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (n.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG) c.2363_2451delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu788=) c.1697_1785delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu566=) | |
| 7 | g.55191748G>A | CA454965593 | EGFR | c.2340G>A (p.Leu780=) c.848G>A c.2499G>A (p.Leu833=) c.*28+18820G>A (n.*28+18820G>A) c.2364G>A (p.Leu788=) c.1698G>A (p.Leu566=) | dbSNP |
| 7 | g.55191748G>C | CA367580124 | EGFR | c.2340G>C (p.Leu780Phe) c.848G>C c.2499G>C (p.Leu833Phe) c.*28+18820G>C (n.*28+18820G>C) c.2364G>C (p.Leu788Phe) c.1698G>C (p.Leu566Phe) | dbSNP |
| 7 | g.55191748G>T | CA367580125 | EGFR | c.2340G>T (p.Leu780Phe) c.848G>T c.2499G>T (p.Leu833Phe) c.*28+18820G>T (n.*28+18820G>T) c.2364G>T (p.Leu788Phe) c.1698G>T (p.Leu566Phe) | ClinVar dbSNP COSMIC |
| 7 | g.55191748_55191749delinsTT | CA891842020 | EGFR | c.2340_2341delinsTT (p.Leu780_Val781delinsPheLeu) c.848_849delinsTT c.2499_2500delinsTT (p.Leu833_Val834delinsPheLeu) c.*28+18820_*28+18821delinsTT (n.*28+18820_*28+18821delinsTT) c.2364_2365delinsTT (p.Leu788_Val789delinsPheLeu) c.1698_1699delinsTT (p.Leu566_Val567delinsPheLeu) |