UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191703_55191716del | CA2682855711 | EGFR | c.2311-16_2311-3del (n.2311-16_2311-3del) c.819-16_819-3del c.2470-16_2470-3del (n.2470-16_2470-3del) c.*28+18775_*28+18788del (n.*28+18775_*28+18788del) c.2335-16_2335-3del (n.2335-16_2335-3del) c.1669-16_1669-3del (n.1669-16_1669-3del) | gnomAD v4 |
| 7 | g.55191713T>A | CA2714936390 | EGFR | c.2311-6T>A (n.2311-6T>A) c.819-6T>A c.2470-6T>A (n.2470-6T>A) c.*28+18785T>A (n.*28+18785T>A) c.2335-6T>A (n.2335-6T>A) c.1669-6T>A (n.1669-6T>A) | dbSNP |
| 7 | g.55191713T>C | CA2714936393 | EGFR | c.2311-6T>C (n.2311-6T>C) c.819-6T>C c.2470-6T>C (n.2470-6T>C) c.*28+18785T>C (n.*28+18785T>C) c.2335-6T>C (n.2335-6T>C) c.1669-6T>C (n.1669-6T>C) | dbSNP |
| 7 | g.55191713T>G | CA2714936397 | EGFR | c.2311-6T>G (n.2311-6T>G) c.819-6T>G c.2470-6T>G (n.2470-6T>G) c.*28+18785T>G (n.*28+18785T>G) c.2335-6T>G (n.2335-6T>G) c.1669-6T>G (n.1669-6T>G) | dbSNP |
| 7 | g.55191714T>A | CA2714936419 | EGFR | c.2311-5T>A (n.2311-5T>A) c.819-5T>A c.2470-5T>A (n.2470-5T>A) c.*28+18786T>A (n.*28+18786T>A) c.2335-5T>A (n.2335-5T>A) c.1669-5T>A (n.1669-5T>A) | dbSNP |
| 7 | g.55191714T>C | CA2714936464 | EGFR | c.2311-5T>C (n.2311-5T>C) c.819-5T>C c.2470-5T>C (n.2470-5T>C) c.*28+18786T>C (n.*28+18786T>C) c.2335-5T>C (n.2335-5T>C) c.1669-5T>C (n.1669-5T>C) | dbSNP |
| 7 | g.55191715T>A | CA2714936519 | EGFR | c.2311-4T>A (n.2311-4T>A) c.819-4T>A c.2470-4T>A (n.2470-4T>A) c.*28+18787T>A (n.*28+18787T>A) c.2335-4T>A (n.2335-4T>A) c.1669-4T>A (n.1669-4T>A) | dbSNP |
| 7 | g.55191715T>C | CA2714936524 | EGFR | c.2311-4T>C (n.2311-4T>C) c.819-4T>C c.2470-4T>C (n.2470-4T>C) c.*28+18787T>C (n.*28+18787T>C) c.2335-4T>C (n.2335-4T>C) c.1669-4T>C (n.1669-4T>C) | dbSNP |
| 7 | g.55191716C>A | CA2714936537 | EGFR | c.2311-3C>A (n.2311-3C>A) c.819-3C>A c.2470-3C>A (n.2470-3C>A) c.*28+18788C>A (n.*28+18788C>A) c.2335-3C>A (n.2335-3C>A) c.1669-3C>A (n.1669-3C>A) | dbSNP |
| 7 | g.55191716C>G | CA2714936543 | EGFR | c.2311-3C>G (n.2311-3C>G) c.819-3C>G c.2470-3C>G (n.2470-3C>G) c.*28+18788C>G (n.*28+18788C>G) c.2335-3C>G (n.2335-3C>G) c.1669-3C>G (n.1669-3C>G) | dbSNP |
| 7 | g.55191716C>T | CA2573142229 | EGFR | c.2311-3C>T (n.2311-3C>T) c.819-3C>T c.2470-3C>T (n.2470-3C>T) c.*28+18788C>T (n.*28+18788C>T) c.2335-3C>T (n.2335-3C>T) c.1669-3C>T (n.1669-3C>T) | ClinVar dbSNP |
| 7 | g.55191717A>C | CA367580054 | EGFR | c.2311-2A>C (n.2311-2A>C) c.819-2A>C c.2470-2A>C (n.2470-2A>C) c.*28+18789A>C (n.*28+18789A>C) c.2335-2A>C (n.2335-2A>C) c.1669-2A>C (n.1669-2A>C) | |
| 7 | g.55191717A>G | CA367580055 | EGFR | c.2311-2A>G (n.2311-2A>G) c.819-2A>G c.2470-2A>G (n.2470-2A>G) c.*28+18789A>G (n.*28+18789A>G) c.2335-2A>G (n.2335-2A>G) c.1669-2A>G (n.1669-2A>G) | dbSNP |
| 7 | g.55191717A>T | CA367580056 | EGFR | c.2311-2A>T (n.2311-2A>T) c.819-2A>T c.2470-2A>T (n.2470-2A>T) c.*28+18789A>T (n.*28+18789A>T) c.2335-2A>T (n.2335-2A>T) c.1669-2A>T (n.1669-2A>T) | dbSNP |
| 7 | g.55191718G>A | CA367580057 | EGFR | c.2311-1G>A (n.2311-1G>A) c.819-1G>A c.2470-1G>A (n.2470-1G>A) c.*28+18790G>A (n.*28+18790G>A) c.2335-1G>A (n.2335-1G>A) c.1669-1G>A (n.1669-1G>A) | dbSNP |
| 7 | g.55191718G>C | CA367580058 | EGFR | c.2311-1G>C (n.2311-1G>C) c.819-1G>C c.2470-1G>C (n.2470-1G>C) c.*28+18790G>C (n.*28+18790G>C) c.2335-1G>C (n.2335-1G>C) c.1669-1G>C (n.1669-1G>C) | dbSNP |
| 7 | g.55191718G>T | CA367580059 | EGFR | c.2311-1G>T (n.2311-1G>T) c.819-1G>T c.2470-1G>T (n.2470-1G>T) c.*28+18790G>T (n.*28+18790G>T) c.2335-1G>T (n.2335-1G>T) c.1669-1G>T (n.1669-1G>T) | dbSNP |
| 7 | g.55191719G>A | CA367580060 | EGFR | c.2311G>A (p.Gly771Ser) c.819G>A c.2470G>A (p.Gly824Ser) c.*28+18791G>A (n.*28+18791G>A) c.2335G>A (p.Gly779Ser) c.1669G>A (p.Gly557Ser) | dbSNP |
| 7 | g.55191719G>C | CA367580061 | EGFR | c.2311G>C (p.Gly771Arg) c.819G>C c.2470G>C (p.Gly824Arg) c.*28+18791G>C (n.*28+18791G>C) c.2335G>C (p.Gly779Arg) c.1669G>C (p.Gly557Arg) | dbSNP |
| 7 | g.55191719G>T | CA367580062 | EGFR | c.2311G>T (p.Gly771Cys) c.819G>T c.2470G>T (p.Gly824Cys) c.*28+18791G>T (n.*28+18791G>T) c.2335G>T (p.Gly779Cys) c.1669G>T (p.Gly557Cys) | dbSNP |
| 7 | g.55191720G>A | CA151169 | EGFR | c.2312G>A (p.Gly771Asp) c.820G>A c.2471G>A (p.Gly824Asp) c.*28+18792G>A (n.*28+18792G>A) c.2336G>A (p.Gly779Asp) c.1670G>A (p.Gly557Asp) | ClinVar dbSNP ExAC gnomAD v2 |
| 7 | g.55191720G>C | CA367580064 | EGFR | c.2312G>C (p.Gly771Ala) c.820G>C c.2471G>C (p.Gly824Ala) c.*28+18792G>C (n.*28+18792G>C) c.2336G>C (p.Gly779Ala) c.1670G>C (p.Gly557Ala) | dbSNP |
| 7 | g.55191720G= | CA1708922380 | EGFR | c.2312G= (p.Gly771=) c.820G= c.2471G= (p.Gly824=) c.*28+18792G= (n.*28+18792G=) c.2336G= (p.Gly779=) c.1670G= (p.Gly557=) | |
| 7 | g.55191720G>T | CA367580063 | EGFR | c.2312G>T (p.Gly771Val) c.820G>T c.2471G>T (p.Gly824Val) c.*28+18792G>T (n.*28+18792G>T) c.2336G>T (p.Gly779Val) c.1670G>T (p.Gly557Val) | dbSNP |
| 7 | g.55191721C>A | CA454965570 | EGFR | c.2313C>A (p.Gly771=) c.821C>A c.2472C>A (p.Gly824=) c.*28+18793C>A (n.*28+18793C>A) c.2337C>A (p.Gly779=) c.1671C>A (p.Gly557=) | COSMIC |
| 7 | g.55191721C>G | CA454965571 | EGFR | c.2313C>G (p.Gly771=) c.821C>G c.2472C>G (p.Gly824=) c.*28+18793C>G (n.*28+18793C>G) c.2337C>G (p.Gly779=) c.1671C>G (p.Gly557=) | dbSNP |
| 7 | g.55191721C>T | CA454965572 | EGFR | c.2313C>T (p.Gly771=) c.821C>T c.2472C>T (p.Gly824=) c.*28+18793C>T (n.*28+18793C>T) c.2337C>T (p.Gly779=) c.1671C>T (p.Gly557=) | dbSNP |
| 7 | g.55191721_55191725del | CA2682855716 | EGFR | c.2313_2317del (p.Met772LeufsTer?) c.821_825del c.2472_2476del (p.Met825LeufsTer?) c.*28+18793_*28+18797del (n.*28+18793_*28+18797del) c.2337_2341del (p.Met780LeufsTer?) c.1671_1675del (p.Met558LeufsTer?) | gnomAD v4 |
| 7 | g.55191722A>C | CA367580065 | EGFR | c.2314A>C (p.Met772Leu) c.822A>C c.2473A>C (p.Met825Leu) c.*28+18794A>C (n.*28+18794A>C) c.2338A>C (p.Met780Leu) c.1672A>C (p.Met558Leu) | ClinVar dbSNP |
| 7 | g.55191722A>G | CA367580066 | EGFR | c.2314A>G (p.Met772Val) c.822A>G c.2473A>G (p.Met825Val) c.*28+18794A>G (n.*28+18794A>G) c.2338A>G (p.Met780Val) c.1672A>G (p.Met558Val) | dbSNP |
| 7 | g.55191722A>T | CA367580067 | EGFR | c.2314A>T (p.Met772Leu) c.822A>T c.2473A>T (p.Met825Leu) c.*28+18794A>T (n.*28+18794A>T) c.2338A>T (p.Met780Leu) c.1672A>T (p.Met558Leu) | dbSNP |
| 7 | g.55191723T>A | CA367580068 | EGFR | c.2315T>A (p.Met772Lys) c.823T>A c.2474T>A (p.Met825Lys) c.*28+18795T>A (n.*28+18795T>A) c.2339T>A (p.Met780Lys) c.1673T>A (p.Met558Lys) | |
| 7 | g.55191723T>C | CA367580069 | EGFR | c.2315T>C (p.Met772Thr) c.823T>C c.2474T>C (p.Met825Thr) c.*28+18795T>C (n.*28+18795T>C) c.2339T>C (p.Met780Thr) c.1673T>C (p.Met558Thr) | dbSNP |
| 7 | g.55191723T>G | CA367580070 | EGFR | c.2315T>G (p.Met772Arg) c.823T>G c.2474T>G (p.Met825Arg) c.*28+18795T>G (n.*28+18795T>G) c.2339T>G (p.Met780Arg) c.1673T>G (p.Met558Arg) | |
| 7 | g.55191724G>A | CA367580071 | EGFR | c.2316G>A (p.Met772Ile) c.824G>A c.2475G>A (p.Met825Ile) c.*28+18796G>A (n.*28+18796G>A) c.2340G>A (p.Met780Ile) c.1674G>A (p.Met558Ile) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55191724G>C | CA367580072 | EGFR | c.2316G>C (p.Met772Ile) c.824G>C c.2475G>C (p.Met825Ile) c.*28+18796G>C (n.*28+18796G>C) c.2340G>C (p.Met780Ile) c.1674G>C (p.Met558Ile) | dbSNP |
| 7 | g.55191724G= | CA1708922388 | EGFR | c.2316G= (p.Met772=) c.824G= c.2475G= (p.Met825=) c.*28+18796G= (n.*28+18796G=) c.2340G= (p.Met780=) c.1674G= (p.Met558=) | |
| 7 | g.55191724G>T | CA367580073 | EGFR | c.2316G>T (p.Met772Ile) c.824G>T c.2475G>T (p.Met825Ile) c.*28+18796G>T (n.*28+18796G>T) c.2340G>T (p.Met780Ile) c.1674G>T (p.Met558Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191725A>C | CA367580074 | EGFR | c.2317A>C (p.Asn773His) c.825A>C c.2476A>C (p.Asn826His) c.*28+18797A>C (n.*28+18797A>C) c.2341A>C (p.Asn781His) c.1675A>C (p.Asn559His) | |
| 7 | g.55191725A>G | CA367580075 | EGFR | c.2317A>G (p.Asn773Asp) c.825A>G c.2476A>G (p.Asn826Asp) c.*28+18797A>G (n.*28+18797A>G) c.2341A>G (p.Asn781Asp) c.1675A>G (p.Asn559Asp) | |
| 7 | g.55191725A>T | CA367580076 | EGFR | c.2317A>T (p.Asn773Tyr) c.825A>T c.2476A>T (p.Asn826Tyr) c.*28+18797A>T (n.*28+18797A>T) c.2341A>T (p.Asn781Tyr) c.1675A>T (p.Asn559Tyr) | |
| 7 | g.55191726A>C | CA367580079 | EGFR | c.2318A>C (p.Asn773Thr) c.826A>C c.2477A>C (p.Asn826Thr) c.*28+18798A>C (n.*28+18798A>C) c.2342A>C (p.Asn781Thr) c.1676A>C (p.Asn559Thr) | dbSNP |
| 7 | g.55191726A>G | CA367580077 | EGFR | c.2318A>G (p.Asn773Ser) c.826A>G c.2477A>G (p.Asn826Ser) c.*28+18798A>G (n.*28+18798A>G) c.2342A>G (p.Asn781Ser) c.1676A>G (p.Asn559Ser) | dbSNP COSMIC |
| 7 | g.55191726A>T | CA367580078 | EGFR | c.2318A>T (p.Asn773Ile) c.826A>T c.2477A>T (p.Asn826Ile) c.*28+18798A>T (n.*28+18798A>T) c.2342A>T (p.Asn781Ile) c.1676A>T (p.Asn559Ile) | dbSNP |
| 7 | g.55191727C>A | CA367580080 | EGFR | c.2319C>A (p.Asn773Lys) c.827C>A c.2478C>A (p.Asn826Lys) c.*28+18799C>A (n.*28+18799C>A) c.2343C>A (p.Asn781Lys) c.1677C>A (p.Asn559Lys) | dbSNP |
| 7 | g.55191727C>G | CA367580081 | EGFR | c.2319C>G (p.Asn773Lys) c.827C>G c.2478C>G (p.Asn826Lys) c.*28+18799C>G (n.*28+18799C>G) c.2343C>G (p.Asn781Lys) c.1677C>G (p.Asn559Lys) | dbSNP |
| 7 | g.55191727C>T | CA454965576 | EGFR | c.2319C>T (p.Asn773=) c.827C>T c.2478C>T (p.Asn826=) c.*28+18799C>T (n.*28+18799C>T) c.2343C>T (p.Asn781=) c.1677C>T (p.Asn559=) | dbSNP |
| 7 | g.55191728T>A | CA367580082 | EGFR | c.2320T>A (p.Tyr774Asn) c.828T>A c.2479T>A (p.Tyr827Asn) c.*28+18800T>A (n.*28+18800T>A) c.2344T>A (p.Tyr782Asn) c.1678T>A (p.Tyr560Asn) | dbSNP |
| 7 | g.55191728T>C | CA367580083 | EGFR | c.2320T>C (p.Tyr774His) c.828T>C c.2479T>C (p.Tyr827His) c.*28+18800T>C (n.*28+18800T>C) c.2344T>C (p.Tyr782His) c.1678T>C (p.Tyr560His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191728T>G | CA367580084 | EGFR | c.2320T>G (p.Tyr774Asp) c.828T>G c.2479T>G (p.Tyr827Asp) c.*28+18800T>G (n.*28+18800T>G) c.2344T>G (p.Tyr782Asp) c.1678T>G (p.Tyr560Asp) | |
| 7 | g.55191728T= | CA1708922393 | EGFR | c.2320T= (p.Tyr774=) c.828T= c.2479T= (p.Tyr827=) c.*28+18800T= (n.*28+18800T=) c.2344T= (p.Tyr782=) c.1678T= (p.Tyr560=) | |
| 7 | g.55191729A= | CA1708922398 | EGFR | c.2321A= (p.Tyr774=) c.829A= c.2480A= (p.Tyr827=) c.*28+18801A= (n.*28+18801A=) c.2345A= (p.Tyr782=) c.1679A= (p.Tyr560=) | |
| 7 | g.55191729A>C | CA367580085 | EGFR | c.2321A>C (p.Tyr774Ser) c.829A>C c.2480A>C (p.Tyr827Ser) c.*28+18801A>C (n.*28+18801A>C) c.2345A>C (p.Tyr782Ser) c.1679A>C (p.Tyr560Ser) | dbSNP |
| 7 | g.55191729A>G | CA367580086 | EGFR | c.2321A>G (p.Tyr774Cys) c.829A>G c.2480A>G (p.Tyr827Cys) c.*28+18801A>G (n.*28+18801A>G) c.2345A>G (p.Tyr782Cys) c.1679A>G (p.Tyr560Cys) | dbSNP |
| 7 | g.55191729A>T | CA158934114 | EGFR | c.2321A>T (p.Tyr774Phe) c.829A>T c.2480A>T (p.Tyr827Phe) c.*28+18801A>T (n.*28+18801A>T) c.2345A>T (p.Tyr782Phe) c.1679A>T (p.Tyr560Phe) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191730C>A | CA367580087 | EGFR | c.2322C>A (p.Tyr774Ter) c.830C>A c.2481C>A (p.Tyr827Ter) c.*28+18802C>A (n.*28+18802C>A) c.2346C>A (p.Tyr782Ter) c.1680C>A (p.Tyr560Ter) | COSMIC |
| 7 | g.55191730C>G | CA367580088 | EGFR | c.2322C>G (p.Tyr774Ter) c.830C>G c.2481C>G (p.Tyr827Ter) c.*28+18802C>G (n.*28+18802C>G) c.2346C>G (p.Tyr782Ter) c.1680C>G (p.Tyr560Ter) | dbSNP |
| 7 | g.55191730C>T | CA454965578 | EGFR | c.2322C>T (p.Tyr774=) c.830C>T c.2481C>T (p.Tyr827=) c.*28+18802C>T (n.*28+18802C>T) c.2346C>T (p.Tyr782=) c.1680C>T (p.Tyr560=) | gnomAD v4 COSMIC |
| 7 | g.55191731T>A | CA367580089 | EGFR | c.2323T>A (p.Leu775Met) c.831T>A c.2482T>A (p.Leu828Met) c.*28+18803T>A (n.*28+18803T>A) c.2347T>A (p.Leu783Met) c.1681T>A (p.Leu561Met) | dbSNP gnomAD v4 |
| 7 | g.55191731T>C | CA454965579 | EGFR | c.2323T>C (p.Leu775=) c.831T>C c.2482T>C (p.Leu828=) c.*28+18803T>C (n.*28+18803T>C) c.2347T>C (p.Leu783=) c.1681T>C (p.Leu561=) | dbSNP gnomAD v4 |
| 7 | g.55191731T>G | CA367580090 | EGFR | c.2323T>G (p.Leu775Val) c.831T>G c.2482T>G (p.Leu828Val) c.*28+18803T>G (n.*28+18803T>G) c.2347T>G (p.Leu783Val) c.1681T>G (p.Leu561Val) | |
| 7 | g.55191732T>A | CA367580092 | EGFR | c.2324T>A (p.Leu775Ter) c.832T>A c.2483T>A (p.Leu828Ter) c.*28+18804T>A (n.*28+18804T>A) c.2348T>A (p.Leu783Ter) c.1682T>A (p.Leu561Ter) | COSMIC |
| 7 | g.55191732T>C | CA367580093 | EGFR | c.2324T>C (p.Leu775Ser) c.832T>C c.2483T>C (p.Leu828Ser) c.*28+18804T>C (n.*28+18804T>C) c.2348T>C (p.Leu783Ser) c.1682T>C (p.Leu561Ser) | |
| 7 | g.55191732T>G | CA367580091 | EGFR | c.2324T>G (p.Leu775Trp) c.832T>G c.2483T>G (p.Leu828Trp) c.*28+18804T>G (n.*28+18804T>G) c.2348T>G (p.Leu783Trp) c.1682T>G (p.Leu561Trp) | |
| 7 | g.55191733G>A | CA180716 | EGFR | c.2325G>A (p.Leu775=) c.833G>A c.2484G>A (p.Leu828=) c.*28+18805G>A (n.*28+18805G>A) c.2349G>A (p.Leu783=) c.1683G>A (p.Leu561=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191733G>C | CA367580094 | EGFR | c.2325G>C (p.Leu775Phe) c.833G>C c.2484G>C (p.Leu828Phe) c.*28+18805G>C (n.*28+18805G>C) c.2349G>C (p.Leu783Phe) c.1683G>C (p.Leu561Phe) | dbSNP |
| 7 | g.55191733G= | CA1708922405 | EGFR | c.2325G= (p.Leu775=) c.833G= c.2484G= (p.Leu828=) c.*28+18805G= (n.*28+18805G=) c.2349G= (p.Leu783=) c.1683G= (p.Leu561=) | |
| 7 | g.55191733G>T | CA367580095 | EGFR | c.2325G>T (p.Leu775Phe) c.833G>T c.2484G>T (p.Leu828Phe) c.*28+18805G>T (n.*28+18805G>T) c.2349G>T (p.Leu783Phe) c.1683G>T (p.Leu561Phe) | dbSNP gnomAD v4 |
| 7 | g.55191734G>A | CA367580096 | EGFR | c.2326G>A (p.Glu776Lys) c.834G>A c.2485G>A (p.Glu829Lys) c.*28+18806G>A (n.*28+18806G>A) c.2350G>A (p.Glu784Lys) c.1684G>A (p.Glu562Lys) | dbSNP COSMIC |
| 7 | g.55191734G>C | CA367580097 | EGFR | c.2326G>C (p.Glu776Gln) c.834G>C c.2485G>C (p.Glu829Gln) c.*28+18806G>C (n.*28+18806G>C) c.2350G>C (p.Glu784Gln) c.1684G>C (p.Glu562Gln) | ClinVar dbSNP |
| 7 | g.55191734G= | CA1708922413 | EGFR | c.2326G= (p.Glu776=) c.834G= c.2485G= (p.Glu829=) c.*28+18806G= (n.*28+18806G=) c.2350G= (p.Glu784=) c.1684G= (p.Glu562=) | |
| 7 | g.55191734G>T | CA367580098 | EGFR | c.2326G>T (p.Glu776Ter) c.834G>T c.2485G>T (p.Glu829Ter) c.*28+18806G>T (n.*28+18806G>T) c.2350G>T (p.Glu784Ter) c.1684G>T (p.Glu562Ter) | dbSNP |
| 7 | g.55191735A>C | CA367580101 | EGFR | c.2327A>C (p.Glu776Ala) c.835A>C c.2486A>C (p.Glu829Ala) c.*28+18807A>C (n.*28+18807A>C) c.2351A>C (p.Glu784Ala) c.1685A>C (p.Glu562Ala) | dbSNP |
| 7 | g.55191735A>G | CA367580100 | EGFR | c.2327A>G (p.Glu776Gly) c.835A>G c.2486A>G (p.Glu829Gly) c.*28+18807A>G (n.*28+18807A>G) c.2351A>G (p.Glu784Gly) c.1685A>G (p.Glu562Gly) | dbSNP |
| 7 | g.55191735A>T | CA367580099 | EGFR | c.2327A>T (p.Glu776Val) c.835A>T c.2486A>T (p.Glu829Val) c.*28+18807A>T (n.*28+18807A>T) c.2351A>T (p.Glu784Val) c.1685A>T (p.Glu562Val) | dbSNP |
| 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) | 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) | |
| 7 | g.55191749del | CA1708922465 | EGFR | c.2341del (p.Val781CysfsTer12) c.849del c.2500del (p.Val834CysfsTer12) c.*28+18821del (n.*28+18821del) c.2365del (p.Val789CysfsTer12) c.1699del (p.Val567CysfsTer12) | dbSNP |
| 7 | g.55191753_55191840del | CA176020 | EGFR | c.2345_2432del (p.His782ArgfsTer?) c.853_899+41del c.2504_2591del (p.His835ArgfsTer?) c.*28+18825_*28+18912del (n.*28+18825_*28+18912del) c.2369_2456del (p.His790ArgfsTer?) c.1703_1790del (p.His568ArgfsTer?) | ClinVar dbSNP |
| 7 | g.55191749G>A | CA367580126 | EGFR | c.2341G>A (p.Val781Met) c.849G>A c.2500G>A (p.Val834Met) c.*28+18821G>A (n.*28+18821G>A) c.2365G>A (p.Val789Met) c.1699G>A (p.Val567Met) | dbSNP COSMIC |
| 7 | g.55191749G>C | CA135917 | EGFR | c.2341G>C (p.Val781Leu) c.849G>C c.2500G>C (p.Val834Leu) c.*28+18821G>C (n.*28+18821G>C) c.2365G>C (p.Val789Leu) c.1699G>C (p.Val567Leu) | ClinVar dbSNP |
| 7 | g.55191749G= | CA1708922471 | EGFR | c.2341G= (p.Val781=) c.849G= c.2500G= (p.Val834=) c.*28+18821G= (n.*28+18821G=) c.2365G= (p.Val789=) c.1699G= (p.Val567=) | |
| 7 | g.55191749G>T | CA135920 | EGFR | c.2341G>T (p.Val781Leu) c.849G>T c.2500G>T (p.Val834Leu) c.*28+18821G>T (n.*28+18821G>T) c.2365G>T (p.Val789Leu) c.1699G>T (p.Val567Leu) | ClinVar dbSNP COSMIC |
| 7 | g.55191749_55191751delinsATT | CA2573051279 | EGFR | c.2341_2343delinsATT (p.Val781Ile) c.849_851delinsATT c.2500_2502delinsATT (p.Val834Ile) c.*28+18821_*28+18823delinsATT (n.*28+18821_*28+18823delinsATT) c.2365_2367delinsATT (p.Val789Ile) c.1699_1701delinsATT (p.Val567Ile) | |
| 7 | g.55191750T>A | CA367580127 | EGFR | c.2342T>A (p.Val781Glu) c.850T>A c.2501T>A (p.Val834Glu) c.*28+18822T>A (n.*28+18822T>A) c.2366T>A (p.Val789Glu) c.1700T>A (p.Val567Glu) | dbSNP |
| 7 | g.55191750T>C | CA367580128 | EGFR | c.2342T>C (p.Val781Ala) c.850T>C c.2501T>C (p.Val834Ala) c.*28+18822T>C (n.*28+18822T>C) c.2366T>C (p.Val789Ala) c.1700T>C (p.Val567Ala) | dbSNP COSMIC |
| 7 | g.55191750T>G | CA367580129 | EGFR | c.2342T>G (p.Val781Gly) c.850T>G c.2501T>G (p.Val834Gly) c.*28+18822T>G (n.*28+18822T>G) c.2366T>G (p.Val789Gly) c.1700T>G (p.Val567Gly) | dbSNP |
| 7 | g.55191751G>A | CA454965594 | EGFR | c.2343G>A (p.Val781=) c.851G>A c.2502G>A (p.Val834=) c.*28+18823G>A (n.*28+18823G>A) c.2367G>A (p.Val789=) c.1701G>A (p.Val567=) | dbSNP |
| 7 | g.55191751G>C | CA454965595 | EGFR | c.2343G>C (p.Val781=) c.851G>C c.2502G>C (p.Val834=) c.*28+18823G>C (n.*28+18823G>C) c.2367G>C (p.Val789=) c.1701G>C (p.Val567=) | dbSNP |
| 7 | g.55191751G>T | CA454965596 | EGFR | c.2343G>T (p.Val781=) c.851G>T c.2502G>T (p.Val834=) c.*28+18823G>T (n.*28+18823G>T) c.2367G>T (p.Val789=) c.1701G>T (p.Val567=) | gnomAD v4 |
| 7 | g.55191752C>A | CA367580132 | EGFR | c.2344C>A (p.His782Asn) c.852C>A c.2503C>A (p.His835Asn) c.*28+18824C>A (n.*28+18824C>A) c.2368C>A (p.His790Asn) c.1702C>A (p.His568Asn) | dbSNP |
| 7 | g.55191752C>G | CA367580130 | EGFR | c.2344C>G (p.His782Asp) c.852C>G c.2503C>G (p.His835Asp) c.*28+18824C>G (n.*28+18824C>G) c.2368C>G (p.His790Asp) c.1702C>G (p.His568Asp) | dbSNP |
| 7 | g.55191752C>T | CA367580131 | EGFR | c.2344C>T (p.His782Tyr) c.852C>T c.2503C>T (p.His835Tyr) c.*28+18824C>T (n.*28+18824C>T) c.2368C>T (p.His790Tyr) c.1702C>T (p.His568Tyr) | dbSNP |
| 7 | g.55191753A= | CA1708922475 | EGFR | c.2345A= (p.His782=) c.853A= c.2504A= (p.His835=) c.*28+18825A= (n.*28+18825A=) c.2369A= (p.His790=) c.1703A= (p.His568=) | |
| 7 | g.55191753A>C | CA367580133 | EGFR | c.2345A>C (p.His782Pro) c.853A>C c.2504A>C (p.His835Pro) c.*28+18825A>C (n.*28+18825A>C) c.2369A>C (p.His790Pro) c.1703A>C (p.His568Pro) | dbSNP |
| 7 | g.55191753A>G | CA367580134 | EGFR | c.2345A>G (p.His782Arg) c.853A>G c.2504A>G (p.His835Arg) c.*28+18825A>G (n.*28+18825A>G) c.2369A>G (p.His790Arg) c.1703A>G (p.His568Arg) | dbSNP |
| 7 | g.55191753A>T | CA135921 | EGFR | c.2345A>T (p.His782Leu) c.853A>T c.2504A>T (p.His835Leu) c.*28+18825A>T (n.*28+18825A>T) c.2369A>T (p.His790Leu) c.1703A>T (p.His568Leu) | ClinVar dbSNP COSMIC |
| 7 | g.55191754C>A | CA367580135 | EGFR | c.2346C>A (p.His782Gln) c.854C>A c.2505C>A (p.His835Gln) c.*28+18826C>A (n.*28+18826C>A) c.2370C>A (p.His790Gln) c.1704C>A (p.His568Gln) | dbSNP |
| 7 | g.55191754C>G | CA367580136 | EGFR | c.2346C>G (p.His782Gln) c.854C>G c.2505C>G (p.His835Gln) c.*28+18826C>G (n.*28+18826C>G) c.2370C>G (p.His790Gln) c.1704C>G (p.His568Gln) | dbSNP |
| 7 | g.55191754C>T | CA454965597 | EGFR | c.2346C>T (p.His782=) c.854C>T c.2505C>T (p.His835=) c.*28+18826C>T (n.*28+18826C>T) c.2370C>T (p.His790=) c.1704C>T (p.His568=) | dbSNP COSMIC |
| 7 | g.55191755C>A | CA367580137 | EGFR | c.2347C>A (p.Arg783Ser) c.855C>A c.2506C>A (p.Arg836Ser) c.*28+18827C>A (n.*28+18827C>A) c.2371C>A (p.Arg791Ser) c.1705C>A (p.Arg569Ser) | dbSNP COSMIC |
| 7 | g.55191755C= | CA1708922481 | EGFR | c.2347C= (p.Arg783=) c.855C= c.2506C= (p.Arg836=) c.*28+18827C= (n.*28+18827C=) c.2371C= (p.Arg791=) c.1705C= (p.Arg569=) | |
| 7 | g.55191755C>G | CA367580138 | EGFR | c.2347C>G (p.Arg783Gly) c.855C>G c.2506C>G (p.Arg836Gly) c.*28+18827C>G (n.*28+18827C>G) c.2371C>G (p.Arg791Gly) c.1705C>G (p.Arg569Gly) | dbSNP |
| 7 | g.55191755C>T | CA4266107 | EGFR | c.2347C>T (p.Arg783Cys) c.855C>T c.2506C>T (p.Arg836Cys) c.*28+18827C>T (n.*28+18827C>T) c.2371C>T (p.Arg791Cys) c.1705C>T (p.Arg569Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191756G>A | CA4266108 | EGFR | c.2348G>A (p.Arg783His) c.856G>A c.2507G>A (p.Arg836His) c.*28+18828G>A (n.*28+18828G>A) c.2372G>A (p.Arg791His) c.1706G>A (p.Arg569His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191756G>C | CA367580139 | EGFR | c.2348G>C (p.Arg783Pro) c.856G>C c.2507G>C (p.Arg836Pro) c.*28+18828G>C (n.*28+18828G>C) c.2372G>C (p.Arg791Pro) c.1706G>C (p.Arg569Pro) | dbSNP |
| 7 | g.55191756G= | CA1708922490 | EGFR | c.2348G= (p.Arg783=) c.856G= c.2507G= (p.Arg836=) c.*28+18828G= (n.*28+18828G=) c.2372G= (p.Arg791=) c.1706G= (p.Arg569=) | |
| 7 | g.55191756G>T | CA367580140 | EGFR | c.2348G>T (p.Arg783Leu) c.856G>T c.2507G>T (p.Arg836Leu) c.*28+18828G>T (n.*28+18828G>T) c.2372G>T (p.Arg791Leu) c.1706G>T (p.Arg569Leu) | |
| 7 | g.55191757C>A | CA454965598 | EGFR | c.2349C>A (p.Arg783=) c.857C>A c.2508C>A (p.Arg836=) c.*28+18829C>A (n.*28+18829C>A) c.2373C>A (p.Arg791=) c.1707C>A (p.Arg569=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191757C= | CA1708922501 | EGFR | c.2349C= (p.Arg783=) c.857C= c.2508C= (p.Arg836=) c.*28+18829C= (n.*28+18829C=) c.2373C= (p.Arg791=) c.1707C= (p.Arg569=) | |
| 7 | g.55191757C>G | CA4266109 | EGFR | c.2349C>G (p.Arg783=) c.857C>G c.2508C>G (p.Arg836=) c.*28+18829C>G (n.*28+18829C>G) c.2373C>G (p.Arg791=) c.1707C>G (p.Arg569=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191757C>T | CA135924 | EGFR | c.2349C>T (p.Arg783=) c.857C>T c.2508C>T (p.Arg836=) c.*28+18829C>T (n.*28+18829C>T) c.2373C>T (p.Arg791=) c.1707C>T (p.Arg569=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191758G>A | CA4266110 | EGFR | c.2350G>A (p.Asp784Asn) c.858G>A c.2509G>A (p.Asp837Asn) c.*28+18830G>A (n.*28+18830G>A) c.2374G>A (p.Asp792Asn) c.1708G>A (p.Asp570Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191758G>C | CA367580142 | EGFR | c.2350G>C (p.Asp784His) c.858G>C c.2509G>C (p.Asp837His) c.*28+18830G>C (n.*28+18830G>C) c.2374G>C (p.Asp792His) c.1708G>C (p.Asp570His) | dbSNP |
| 7 | g.55191758G= | CA1708922508 | EGFR | c.2350G= (p.Asp784=) c.858G= c.2509G= (p.Asp837=) c.*28+18830G= (n.*28+18830G=) c.2374G= (p.Asp792=) c.1708G= (p.Asp570=) | |
| 7 | g.55191758G>T | CA367580141 | EGFR | c.2350G>T (p.Asp784Tyr) c.858G>T c.2509G>T (p.Asp837Tyr) c.*28+18830G>T (n.*28+18830G>T) c.2374G>T (p.Asp792Tyr) c.1708G>T (p.Asp570Tyr) | dbSNP gnomAD v4 |
| 7 | g.55191759A= | CA1708922512 | EGFR | c.2351A= (p.Asp784=) c.859A= c.2510A= (p.Asp837=) c.*28+18831A= (n.*28+18831A=) c.2375A= (p.Asp792=) c.1709A= (p.Asp570=) | |
| 7 | g.55191759A>C | CA367580143 | EGFR | c.2351A>C (p.Asp784Ala) c.859A>C c.2510A>C (p.Asp837Ala) c.*28+18831A>C (n.*28+18831A>C) c.2375A>C (p.Asp792Ala) c.1709A>C (p.Asp570Ala) | dbSNP |
| 7 | g.55191759A>G | CA367580144 | EGFR | c.2351A>G (p.Asp784Gly) c.859A>G c.2510A>G (p.Asp837Gly) c.*28+18831A>G (n.*28+18831A>G) c.2375A>G (p.Asp792Gly) c.1709A>G (p.Asp570Gly) | dbSNP COSMIC |
| 7 | g.55191759A>T | CA367580145 | EGFR | c.2351A>T (p.Asp784Val) c.859A>T c.2510A>T (p.Asp837Val) c.*28+18831A>T (n.*28+18831A>T) c.2375A>T (p.Asp792Val) c.1709A>T (p.Asp570Val) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191760C>A | CA367580146 | EGFR | c.2352C>A (p.Asp784Glu) c.860C>A c.2511C>A (p.Asp837Glu) c.*28+18832C>A (n.*28+18832C>A) c.2376C>A (p.Asp792Glu) c.1710C>A (p.Asp570Glu) | |
| 7 | g.55191760C>G | CA367580147 | EGFR | c.2352C>G (p.Asp784Glu) c.860C>G c.2511C>G (p.Asp837Glu) c.*28+18832C>G (n.*28+18832C>G) c.2376C>G (p.Asp792Glu) c.1710C>G (p.Asp570Glu) | dbSNP |
| 7 | g.55191760C>T | CA454965599 | EGFR | c.2352C>T (p.Asp784=) c.860C>T c.2511C>T (p.Asp837=) c.*28+18832C>T (n.*28+18832C>T) c.2376C>T (p.Asp792=) c.1710C>T (p.Asp570=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191761C>A | CA367580148 | EGFR | c.2353C>A (p.Leu785Met) c.861C>A c.2512C>A (p.Leu838Met) c.*28+18833C>A (n.*28+18833C>A) c.2377C>A (p.Leu793Met) c.1711C>A (p.Leu571Met) | dbSNP COSMIC |
| 7 | g.55191761C= | CA1708922520 | EGFR | c.2353C= (p.Leu785=) c.861C= c.2512C= (p.Leu838=) c.*28+18833C= (n.*28+18833C=) c.2377C= (p.Leu793=) c.1711C= (p.Leu571=) | |
| 7 | g.55191761C>G | CA350916 | EGFR | c.2353C>G (p.Leu785Val) c.861C>G c.2512C>G (p.Leu838Val) c.*28+18833C>G (n.*28+18833C>G) c.2377C>G (p.Leu793Val) c.1711C>G (p.Leu571Val) | ClinVar dbSNP COSMIC |
| 7 | g.55191761C>T | CA454965600 | EGFR | c.2353C>T (p.Leu785=) c.861C>T c.2512C>T (p.Leu838=) c.*28+18833C>T (n.*28+18833C>T) c.2377C>T (p.Leu793=) c.1711C>T (p.Leu571=) | dbSNP |
| 7 | g.55191762T>A | CA367580149 | EGFR | c.2354T>A (p.Leu785Gln) c.862T>A c.2513T>A (p.Leu838Gln) c.*28+18834T>A (n.*28+18834T>A) c.2378T>A (p.Leu793Gln) c.1712T>A (p.Leu571Gln) | |
| 7 | g.55191762T>C | CA367580150 | EGFR | c.2354T>C (p.Leu785Pro) c.862T>C c.2513T>C (p.Leu838Pro) c.*28+18834T>C (n.*28+18834T>C) c.2378T>C (p.Leu793Pro) c.1712T>C (p.Leu571Pro) | COSMIC |
| 7 | g.55191762T>G | CA367580151 | EGFR | c.2354T>G (p.Leu785Arg) c.862T>G c.2513T>G (p.Leu838Arg) c.*28+18834T>G (n.*28+18834T>G) c.2378T>G (p.Leu793Arg) c.1712T>G (p.Leu571Arg) | |
| 7 | g.55191763G>A | CA454965601 | EGFR | c.2355G>A (p.Leu785=) c.863G>A c.2514G>A (p.Leu838=) c.*28+18835G>A (n.*28+18835G>A) c.2379G>A (p.Leu793=) c.1713G>A (p.Leu571=) | dbSNP |
| 7 | g.55191763G>C | CA454965602 | EGFR | c.2355G>C (p.Leu785=) c.863G>C c.2514G>C (p.Leu838=) c.*28+18835G>C (n.*28+18835G>C) c.2379G>C (p.Leu793=) c.1713G>C (p.Leu571=) | dbSNP |
| 7 | g.55191763G>T | CA454965604 | EGFR | c.2355G>T (p.Leu785=) c.863G>T c.2514G>T (p.Leu838=) c.*28+18835G>T (n.*28+18835G>T) c.2379G>T (p.Leu793=) c.1713G>T (p.Leu571=) | gnomAD v4 |
| 7 | g.55191764G>A | CA367580152 | EGFR | c.2356G>A (p.Ala786Thr) c.864G>A c.2515G>A (p.Ala839Thr) c.*28+18836G>A (n.*28+18836G>A) c.2380G>A (p.Ala794Thr) c.1714G>A (p.Ala572Thr) | dbSNP COSMIC |
| 7 | g.55191764G>C | CA367580153 | EGFR | c.2356G>C (p.Ala786Pro) c.864G>C c.2515G>C (p.Ala839Pro) c.*28+18836G>C (n.*28+18836G>C) c.2380G>C (p.Ala794Pro) c.1714G>C (p.Ala572Pro) | dbSNP |
| 7 | g.55191764G>T | CA367580154 | EGFR | c.2356G>T (p.Ala786Ser) c.864G>T c.2515G>T (p.Ala839Ser) c.*28+18836G>T (n.*28+18836G>T) c.2380G>T (p.Ala794Ser) c.1714G>T (p.Ala572Ser) | dbSNP |
| 7 | g.55191765C>A | CA367580155 | EGFR | c.2357C>A (p.Ala786Glu) c.865C>A c.2516C>A (p.Ala839Glu) c.*28+18837C>A (n.*28+18837C>A) c.2381C>A (p.Ala794Glu) c.1715C>A (p.Ala572Glu) | |
| 7 | g.55191765C>G | CA367580157 | EGFR | c.2357C>G (p.Ala786Gly) c.865C>G c.2516C>G (p.Ala839Gly) c.*28+18837C>G (n.*28+18837C>G) c.2381C>G (p.Ala794Gly) c.1715C>G (p.Ala572Gly) | dbSNP |
| 7 | g.55191765C>T | CA367580156 | EGFR | c.2357C>T (p.Ala786Val) c.865C>T c.2516C>T (p.Ala839Val) c.*28+18837C>T (n.*28+18837C>T) c.2381C>T (p.Ala794Val) c.1715C>T (p.Ala572Val) | dbSNP COSMIC |
| 7 | g.55191766A>C | CA454965605 | EGFR | c.2358A>C (p.Ala786=) c.866A>C c.2517A>C (p.Ala839=) c.*28+18838A>C (n.*28+18838A>C) c.2382A>C (p.Ala794=) c.1716A>C (p.Ala572=) | gnomAD v4 |
| 7 | g.55191766A>G | CA454965607 | EGFR | c.2358A>G (p.Ala786=) c.866A>G c.2517A>G (p.Ala839=) c.*28+18838A>G (n.*28+18838A>G) c.2382A>G (p.Ala794=) c.1716A>G (p.Ala572=) | |
| 7 | g.55191766A>T | CA454965606 | EGFR | c.2358A>T (p.Ala786=) c.866A>T c.2517A>T (p.Ala839=) c.*28+18838A>T (n.*28+18838A>T) c.2382A>T (p.Ala794=) c.1716A>T (p.Ala572=) | dbSNP |
| 7 | g.55191767G>A | CA4266111 | EGFR | c.2359G>A (p.Ala787Thr) c.867G>A c.2518G>A (p.Ala840Thr) c.*28+18839G>A (n.*28+18839G>A) c.2383G>A (p.Ala795Thr) c.1717G>A (p.Ala573Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191767G>C | CA367580158 | EGFR | c.2359G>C (p.Ala787Pro) c.867G>C c.2518G>C (p.Ala840Pro) c.*28+18839G>C (n.*28+18839G>C) c.2383G>C (p.Ala795Pro) c.1717G>C (p.Ala573Pro) | |
| 7 | g.55191767G= | CA1708922525 | EGFR | c.2359G= (p.Ala787=) c.867G= c.2518G= (p.Ala840=) c.*28+18839G= (n.*28+18839G=) c.2383G= (p.Ala795=) c.1717G= (p.Ala573=) | |
| 7 | g.55191767G>T | CA367580159 | EGFR | c.2359G>T (p.Ala787Ser) c.867G>T c.2518G>T (p.Ala840Ser) c.*28+18839G>T (n.*28+18839G>T) c.2383G>T (p.Ala795Ser) c.1717G>T (p.Ala573Ser) | |
| 7 | g.55191768C>A | CA367580160 | EGFR | c.2360C>A (p.Ala787Asp) c.868C>A c.2519C>A (p.Ala840Asp) c.*28+18840C>A (n.*28+18840C>A) c.2384C>A (p.Ala795Asp) c.1718C>A (p.Ala573Asp) | dbSNP |
| 7 | g.55191768C>G | CA367580161 | EGFR | c.2360C>G (p.Ala787Gly) c.868C>G c.2519C>G (p.Ala840Gly) c.*28+18840C>G (n.*28+18840C>G) c.2384C>G (p.Ala795Gly) c.1718C>G (p.Ala573Gly) | dbSNP gnomAD v4 |
| 7 | g.55191768C>T | CA367580162 | EGFR | c.2360C>T (p.Ala787Val) c.868C>T c.2519C>T (p.Ala840Val) c.*28+18840C>T (n.*28+18840C>T) c.2384C>T (p.Ala795Val) c.1718C>T (p.Ala573Val) | dbSNP |
| 7 | g.55191769C>A | CA454965608 | EGFR | c.2361C>A (p.Ala787=) c.869C>A c.2520C>A (p.Ala840=) c.*28+18841C>A (n.*28+18841C>A) c.2385C>A (p.Ala795=) c.1719C>A (p.Ala573=) | |
| 7 | g.55191769C>G | CA454965609 | EGFR | c.2361C>G (p.Ala787=) c.869C>G c.2520C>G (p.Ala840=) c.*28+18841C>G (n.*28+18841C>G) c.2385C>G (p.Ala795=) c.1719C>G (p.Ala573=) | dbSNP |
| 7 | g.55191769C>T | CA454965610 | EGFR | c.2361C>T (p.Ala787=) c.869C>T c.2520C>T (p.Ala840=) c.*28+18841C>T (n.*28+18841C>T) c.2385C>T (p.Ala795=) c.1719C>T (p.Ala573=) | dbSNP COSMIC |
| 7 | g.55191770A>C | CA454965611 | EGFR | c.2362A>C (p.Arg788=) c.870A>C c.2521A>C (p.Arg841=) c.*28+18842A>C (n.*28+18842A>C) c.2386A>C (p.Arg796=) c.1720A>C (p.Arg574=) | |
| 7 | g.55191770A>G | CA367580163 | EGFR | c.2362A>G (p.Arg788Gly) c.870A>G c.2521A>G (p.Arg841Gly) c.*28+18842A>G (n.*28+18842A>G) c.2386A>G (p.Arg796Gly) c.1720A>G (p.Arg574Gly) | |
| 7 | g.55191770A>T | CA367580164 | EGFR | c.2362A>T (p.Arg788Trp) c.870A>T c.2521A>T (p.Arg841Trp) c.*28+18842A>T (n.*28+18842A>T) c.2386A>T (p.Arg796Trp) c.1720A>T (p.Arg574Trp) | dbSNP |
| 7 | g.55191771G>A | CA367580165 | EGFR | c.2363G>A (p.Arg788Lys) c.871G>A c.2522G>A (p.Arg841Lys) c.*28+18843G>A (n.*28+18843G>A) c.2387G>A (p.Arg796Lys) c.1721G>A (p.Arg574Lys) | COSMIC |
| 7 | g.55191771G>C | CA367580166 | EGFR | c.2363G>C (p.Arg788Thr) c.871G>C c.2522G>C (p.Arg841Thr) c.*28+18843G>C (n.*28+18843G>C) c.2387G>C (p.Arg796Thr) c.1721G>C (p.Arg574Thr) | |
| 7 | g.55191771G>T | CA367580167 | EGFR | c.2363G>T (p.Arg788Met) c.871G>T c.2522G>T (p.Arg841Met) c.*28+18843G>T (n.*28+18843G>T) c.2387G>T (p.Arg796Met) c.1721G>T (p.Arg574Met) | |
| 7 | g.55191772G>A | CA454965612 | EGFR | c.2364G>A (p.Arg788=) c.872G>A c.2523G>A (p.Arg841=) c.*28+18844G>A (n.*28+18844G>A) c.2388G>A (p.Arg796=) c.1722G>A (p.Arg574=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191772G>C | CA4266112 | EGFR | c.2364G>C (p.Arg788Ser) c.872G>C c.2523G>C (p.Arg841Ser) c.*28+18844G>C (n.*28+18844G>C) c.2388G>C (p.Arg796Ser) c.1722G>C (p.Arg574Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55191772G= | CA1708922531 | EGFR | c.2364G= (p.Arg788=) c.872G= c.2523G= (p.Arg841=) c.*28+18844G= (n.*28+18844G=) c.2388G= (p.Arg796=) c.1722G= (p.Arg574=) | |
| 7 | g.55191772G>T | CA367580168 | EGFR | c.2364G>T (p.Arg788Ser) c.872G>T c.2523G>T (p.Arg841Ser) c.*28+18844G>T (n.*28+18844G>T) c.2388G>T (p.Arg796Ser) c.1722G>T (p.Arg574Ser) | dbSNP |
| 7 | g.55191773A= | CA1708922535 | EGFR | c.2365A= (p.Asn789=) c.873A= c.2524A= (p.Asn842=) c.*28+18845A= (n.*28+18845A=) c.2389A= (p.Asn797=) c.1723A= (p.Asn575=) | |
| 7 | g.55191773A>C | CA367580169 | EGFR | c.2365A>C (p.Asn789His) c.873A>C c.2524A>C (p.Asn842His) c.*28+18845A>C (n.*28+18845A>C) c.2389A>C (p.Asn797His) c.1723A>C (p.Asn575His) | dbSNP COSMIC |
| 7 | g.55191773A>G | CA158934194 | EGFR | c.2365A>G (p.Asn789Asp) c.873A>G c.2524A>G (p.Asn842Asp) c.*28+18845A>G (n.*28+18845A>G) c.2389A>G (p.Asn797Asp) c.1723A>G (p.Asn575Asp) | ClinVar dbSNP COSMIC |
| 7 | g.55191773A>T | CA367580170 | EGFR | c.2365A>T (p.Asn789Tyr) c.873A>T c.2524A>T (p.Asn842Tyr) c.*28+18845A>T (n.*28+18845A>T) c.2389A>T (p.Asn797Tyr) c.1723A>T (p.Asn575Tyr) | dbSNP |
| 7 | g.55191774A>C | CA367580171 | EGFR | c.2366A>C (p.Asn789Thr) c.874A>C c.2525A>C (p.Asn842Thr) c.*28+18846A>C (n.*28+18846A>C) c.2390A>C (p.Asn797Thr) c.1724A>C (p.Asn575Thr) | dbSNP |
| 7 | g.55191774A>G | CA367580172 | EGFR | c.2366A>G (p.Asn789Ser) c.874A>G c.2525A>G (p.Asn842Ser) c.*28+18846A>G (n.*28+18846A>G) c.2390A>G (p.Asn797Ser) c.1724A>G (p.Asn575Ser) | dbSNP |
| 7 | g.55191774A>T | CA367580173 | EGFR | c.2366A>T (p.Asn789Ile) c.874A>T c.2525A>T (p.Asn842Ile) c.*28+18846A>T (n.*28+18846A>T) c.2390A>T (p.Asn797Ile) c.1724A>T (p.Asn575Ile) | dbSNP |
| 7 | g.55191775C>A | CA367580174 | EGFR | c.2367C>A (p.Asn789Lys) c.875C>A c.2526C>A (p.Asn842Lys) c.*28+18847C>A (n.*28+18847C>A) c.2391C>A (p.Asn797Lys) c.1725C>A (p.Asn575Lys) | dbSNP |
| 7 | g.55191775C= | CA1708922541 | EGFR | c.2367C= (p.Asn789=) c.875C= c.2526C= (p.Asn842=) c.*28+18847C= (n.*28+18847C=) c.2391C= (p.Asn797=) c.1725C= (p.Asn575=) | |
| 7 | g.55191775C>G | CA367580175 | EGFR | c.2367C>G (p.Asn789Lys) c.875C>G c.2526C>G (p.Asn842Lys) c.*28+18847C>G (n.*28+18847C>G) c.2391C>G (p.Asn797Lys) c.1725C>G (p.Asn575Lys) | dbSNP |
| 7 | g.55191775C>T | CA454965615 | EGFR | c.2367C>T (p.Asn789=) c.875C>T c.2526C>T (p.Asn842=) c.*28+18847C>T (n.*28+18847C>T) c.2391C>T (p.Asn797=) c.1725C>T (p.Asn575=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191776G>A | CA16602666 | EGFR | c.2368G>A (p.Val790Ile) c.876G>A c.2527G>A (p.Val843Ile) c.*28+18848G>A (n.*28+18848G>A) c.2392G>A (p.Val798Ile) c.1726G>A (p.Val576Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191776G>C | CA367580176 | EGFR | c.2368G>C (p.Val790Leu) c.876G>C c.2527G>C (p.Val843Leu) c.*28+18848G>C (n.*28+18848G>C) c.2392G>C (p.Val798Leu) c.1726G>C (p.Val576Leu) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55191776G= | CA1708922547 | EGFR | c.2368G= (p.Val790=) c.876G= c.2527G= (p.Val843=) c.*28+18848G= (n.*28+18848G=) c.2392G= (p.Val798=) c.1726G= (p.Val576=) | |
| 7 | g.55191776G>T | CA367580177 | EGFR | c.2368G>T (p.Val790Leu) c.876G>T c.2527G>T (p.Val843Leu) c.*28+18848G>T (n.*28+18848G>T) c.2392G>T (p.Val798Leu) c.1726G>T (p.Val576Leu) | COSMIC |
| 7 | g.55191777T>A | CA367580178 | EGFR | c.2369T>A (p.Val790Glu) c.877T>A c.2528T>A (p.Val843Glu) c.*28+18849T>A (n.*28+18849T>A) c.2393T>A (p.Val798Glu) c.1727T>A (p.Val576Glu) | dbSNP |
| 7 | g.55191777T>C | CA367580179 | EGFR | c.2369T>C (p.Val790Ala) c.877T>C c.2528T>C (p.Val843Ala) c.*28+18849T>C (n.*28+18849T>C) c.2393T>C (p.Val798Ala) c.1727T>C (p.Val576Ala) | dbSNP |
| 7 | g.55191777T>G | CA367580180 | EGFR | c.2369T>G (p.Val790Gly) c.877T>G c.2528T>G (p.Val843Gly) c.*28+18849T>G (n.*28+18849T>G) c.2393T>G (p.Val798Gly) c.1727T>G (p.Val576Gly) | dbSNP |
| 7 | g.55191778A>C | CA454965616 | EGFR | c.2370A>C (p.Val790=) c.878A>C c.2529A>C (p.Val843=) c.*28+18850A>C (n.*28+18850A>C) c.2394A>C (p.Val798=) c.1728A>C (p.Val576=) | dbSNP |
| 7 | g.55191778A>G | CA454965617 | EGFR | c.2370A>G (p.Val790=) c.878A>G c.2529A>G (p.Val843=) c.*28+18850A>G (n.*28+18850A>G) c.2394A>G (p.Val798=) c.1728A>G (p.Val576=) | ClinVar |
| 7 | g.55191778A>T | CA454965618 | EGFR | c.2370A>T (p.Val790=) c.878A>T c.2529A>T (p.Val843=) c.*28+18850A>T (n.*28+18850A>T) c.2394A>T (p.Val798=) c.1728A>T (p.Val576=) | dbSNP |
| 7 | g.55191779C>A | CA367580181 | EGFR | c.2371C>A (p.Leu791Met) c.879C>A c.2530C>A (p.Leu844Met) c.*28+18851C>A (n.*28+18851C>A) c.2395C>A (p.Leu799Met) c.1729C>A (p.Leu577Met) | dbSNP |
| 7 | g.55191779C>G | CA367580182 | EGFR | c.2371C>G (p.Leu791Val) c.879C>G c.2530C>G (p.Leu844Val) c.*28+18851C>G (n.*28+18851C>G) c.2395C>G (p.Leu799Val) c.1729C>G (p.Leu577Val) | dbSNP COSMIC |
| 7 | g.55191779C>T | CA454965619 | EGFR | c.2371C>T (p.Leu791=) c.879C>T c.2530C>T (p.Leu844=) c.*28+18851C>T (n.*28+18851C>T) c.2395C>T (p.Leu799=) c.1729C>T (p.Leu577=) | dbSNP |
| 7 | g.55191780T>A | CA367580183 | EGFR | c.2372T>A (p.Leu791Gln) c.880T>A c.2531T>A (p.Leu844Gln) c.*28+18852T>A (n.*28+18852T>A) c.2396T>A (p.Leu799Gln) c.1730T>A (p.Leu577Gln) | |
| 7 | g.55191780T>C | CA367580184 | EGFR | c.2372T>C (p.Leu791Pro) c.880T>C c.2531T>C (p.Leu844Pro) c.*28+18852T>C (n.*28+18852T>C) c.2396T>C (p.Leu799Pro) c.1730T>C (p.Leu577Pro) | COSMIC |
| 7 | g.55191780T>G | CA367580185 | EGFR | c.2372T>G (p.Leu791Arg) c.880T>G c.2531T>G (p.Leu844Arg) c.*28+18852T>G (n.*28+18852T>G) c.2396T>G (p.Leu799Arg) c.1730T>G (p.Leu577Arg) | |
| 7 | g.55191781G>A | CA454965620 | EGFR | c.2373G>A (p.Leu791=) c.881G>A c.2532G>A (p.Leu844=) c.*28+18853G>A (n.*28+18853G>A) c.2397G>A (p.Leu799=) c.1731G>A (p.Leu577=) | dbSNP gnomAD v4 |
| 7 | g.55191781G>C | CA454965621 | EGFR | c.2373G>C (p.Leu791=) c.881G>C c.2532G>C (p.Leu844=) c.*28+18853G>C (n.*28+18853G>C) c.2397G>C (p.Leu799=) c.1731G>C (p.Leu577=) | dbSNP |
| 7 | g.55191781G>T | CA454965622 | EGFR | c.2373G>T (p.Leu791=) c.881G>T c.2532G>T (p.Leu844=) c.*28+18853G>T (n.*28+18853G>T) c.2397G>T (p.Leu799=) c.1731G>T (p.Leu577=) | dbSNP |
| 7 | g.55191782G>A | CA367580186 | EGFR | c.2374G>A (p.Val792Met) c.882G>A c.2533G>A (p.Val845Met) c.*28+18854G>A (n.*28+18854G>A) c.2398G>A (p.Val800Met) c.1732G>A (p.Val578Met) | ClinVar dbSNP COSMIC |
| 7 | g.55191782G>C | CA367580187 | EGFR | c.2374G>C (p.Val792Leu) c.882G>C c.2533G>C (p.Val845Leu) c.*28+18854G>C (n.*28+18854G>C) c.2398G>C (p.Val800Leu) c.1732G>C (p.Val578Leu) | ClinVar dbSNP |
| 7 | g.55191782G= | CA1708922554 | EGFR | c.2374G= (p.Val792=) c.882G= c.2533G= (p.Val845=) c.*28+18854G= (n.*28+18854G=) c.2398G= (p.Val800=) c.1732G= (p.Val578=) | |
| 7 | g.55191782G>T | CA367580188 | EGFR | c.2374G>T (p.Val792Leu) c.882G>T c.2533G>T (p.Val845Leu) c.*28+18854G>T (n.*28+18854G>T) c.2398G>T (p.Val800Leu) c.1732G>T (p.Val578Leu) | dbSNP |
| 7 | g.55191783T>A | CA367580189 | EGFR | c.2375T>A (p.Val792Glu) c.883T>A c.2534T>A (p.Val845Glu) c.*28+18855T>A (n.*28+18855T>A) c.2399T>A (p.Val800Glu) c.1733T>A (p.Val578Glu) | |
| 7 | g.55191783T>C | CA367580190 | EGFR | c.2375T>C (p.Val792Ala) c.883T>C c.2534T>C (p.Val845Ala) c.*28+18855T>C (n.*28+18855T>C) c.2399T>C (p.Val800Ala) c.1733T>C (p.Val578Ala) | COSMIC |
| 7 | g.55191783T>G | CA367580191 | EGFR | c.2375T>G (p.Val792Gly) c.883T>G c.2534T>G (p.Val845Gly) c.*28+18855T>G (n.*28+18855T>G) c.2399T>G (p.Val800Gly) c.1733T>G (p.Val578Gly) | dbSNP |
| 7 | g.55191784G>A | CA454965623 | EGFR | c.2376G>A (p.Val792=) c.884G>A c.2535G>A (p.Val845=) c.*28+18856G>A (n.*28+18856G>A) c.2400G>A (p.Val800=) c.1734G>A (p.Val578=) | |
| 7 | g.55191784G>C | CA454965624 | EGFR | c.2376G>C (p.Val792=) c.884G>C c.2535G>C (p.Val845=) c.*28+18856G>C (n.*28+18856G>C) c.2400G>C (p.Val800=) c.1734G>C (p.Val578=) | |
| 7 | g.55191784G>T | CA454965625 | EGFR | c.2376G>T (p.Val792=) c.884G>T c.2535G>T (p.Val845=) c.*28+18856G>T (n.*28+18856G>T) c.2400G>T (p.Val800=) c.1734G>T (p.Val578=) | |
| 7 | g.55191785A>C | CA367580192 | EGFR | c.2377A>C (p.Lys793Gln) c.885A>C c.2536A>C (p.Lys846Gln) c.*28+18857A>C (n.*28+18857A>C) c.2401A>C (p.Lys801Gln) c.1735A>C (p.Lys579Gln) | |
| 7 | g.55191785A>G | CA367580193 | EGFR | c.2377A>G (p.Lys793Glu) c.885A>G c.2536A>G (p.Lys846Glu) c.*28+18857A>G (n.*28+18857A>G) c.2401A>G (p.Lys801Glu) c.1735A>G (p.Lys579Glu) | dbSNP |
| 7 | g.55191785A>T | CA367580194 | EGFR | c.2377A>T (p.Lys793Ter) c.885A>T c.2536A>T (p.Lys846Ter) c.*28+18857A>T (n.*28+18857A>T) c.2401A>T (p.Lys801Ter) c.1735A>T (p.Lys579Ter) | |
| 7 | g.55191786A= | CA1708922557 | EGFR | c.2378A= (p.Lys793=) c.886A= c.2537A= (p.Lys846=) c.*28+18858A= (n.*28+18858A=) c.2402A= (p.Lys801=) c.1736A= (p.Lys579=) | |
| 7 | g.55191786A>C | CA367580197 | EGFR | c.2378A>C (p.Lys793Thr) c.886A>C c.2537A>C (p.Lys846Thr) c.*28+18858A>C (n.*28+18858A>C) c.2402A>C (p.Lys801Thr) c.1736A>C (p.Lys579Thr) | |
| 7 | g.55191786A>G | CA367580196 | EGFR | c.2378A>G (p.Lys793Arg) c.886A>G c.2537A>G (p.Lys846Arg) c.*28+18858A>G (n.*28+18858A>G) c.2402A>G (p.Lys801Arg) c.1736A>G (p.Lys579Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191786A>T | CA367580195 | EGFR | c.2378A>T (p.Lys793Ile) c.886A>T c.2537A>T (p.Lys846Ile) c.*28+18858A>T (n.*28+18858A>T) c.2402A>T (p.Lys801Ile) c.1736A>T (p.Lys579Ile) | dbSNP |
| 7 | g.55191787A>C | CA367580198 | EGFR | c.2379A>C (p.Lys793Asn) c.887A>C c.2538A>C (p.Lys846Asn) c.*28+18859A>C (n.*28+18859A>C) c.2403A>C (p.Lys801Asn) c.1737A>C (p.Lys579Asn) | dbSNP |
| 7 | g.55191787A>G | CA454965626 | EGFR | c.2379A>G (p.Lys793=) c.887A>G c.2538A>G (p.Lys846=) c.*28+18859A>G (n.*28+18859A>G) c.2403A>G (p.Lys801=) c.1737A>G (p.Lys579=) | |
| 7 | g.55191787A>T | CA367580199 | EGFR | c.2379A>T (p.Lys793Asn) c.887A>T c.2538A>T (p.Lys846Asn) c.*28+18859A>T (n.*28+18859A>T) c.2403A>T (p.Lys801Asn) c.1737A>T (p.Lys579Asn) | dbSNP |
| 7 | g.55191788A>C | CA367580200 | EGFR | c.2380A>C (p.Thr794Pro) c.888A>C c.2539A>C (p.Thr847Pro) c.*28+18860A>C (n.*28+18860A>C) c.2404A>C (p.Thr802Pro) c.1738A>C (p.Thr580Pro) | dbSNP |
| 7 | g.55191788A>G | CA367580202 | EGFR | c.2380A>G (p.Thr794Ala) c.888A>G c.2539A>G (p.Thr847Ala) c.*28+18860A>G (n.*28+18860A>G) c.2404A>G (p.Thr802Ala) c.1738A>G (p.Thr580Ala) | dbSNP |
| 7 | g.55191788A>T | CA367580201 | EGFR | c.2380A>T (p.Thr794Ser) c.888A>T c.2539A>T (p.Thr847Ser) c.*28+18860A>T (n.*28+18860A>T) c.2404A>T (p.Thr802Ser) c.1738A>T (p.Thr580Ser) | dbSNP |
| 7 | g.55191789C>A | CA367580203 | EGFR | c.2381C>A (p.Thr794Lys) c.889C>A c.2540C>A (p.Thr847Lys) c.*28+18861C>A (n.*28+18861C>A) c.2405C>A (p.Thr802Lys) c.1739C>A (p.Thr580Lys) | dbSNP |
| 7 | g.55191789C= | CA1708922559 | EGFR | c.2381C= (p.Thr794=) c.889C= c.2540C= (p.Thr847=) c.*28+18861C= (n.*28+18861C=) c.2405C= (p.Thr802=) c.1739C= (p.Thr580=) | |
| 7 | g.55191789C>G | CA367580205 | EGFR | c.2381C>G (p.Thr794Arg) c.889C>G c.2540C>G (p.Thr847Arg) c.*28+18861C>G (n.*28+18861C>G) c.2405C>G (p.Thr802Arg) c.1739C>G (p.Thr580Arg) | dbSNP |
| 7 | g.55191789C>T | CA367580204 | EGFR | c.2381C>T (p.Thr794Ile) c.889C>T c.2540C>T (p.Thr847Ile) c.*28+18861C>T (n.*28+18861C>T) c.2405C>T (p.Thr802Ile) c.1739C>T (p.Thr580Ile) | dbSNP COSMIC |
| 7 | g.55191790A>C | CA454965627 | EGFR | c.2382A>C (p.Thr794=) c.890A>C c.2541A>C (p.Thr847=) c.*28+18862A>C (n.*28+18862A>C) c.2406A>C (p.Thr802=) c.1740A>C (p.Thr580=) | dbSNP |
| 7 | g.55191790A>G | CA454965628 | EGFR | c.2382A>G (p.Thr794=) c.890A>G c.2541A>G (p.Thr847=) c.*28+18862A>G (n.*28+18862A>G) c.2406A>G (p.Thr802=) c.1740A>G (p.Thr580=) | dbSNP |
| 7 | g.55191790A>T | CA454965629 | EGFR | c.2382A>T (p.Thr794=) c.890A>T c.2541A>T (p.Thr847=) c.*28+18862A>T (n.*28+18862A>T) c.2406A>T (p.Thr802=) c.1740A>T (p.Thr580=) | dbSNP |
| 7 | g.55191791C>A | CA367580206 | EGFR | c.2383C>A (p.Pro795Thr) c.891C>A c.2542C>A (p.Pro848Thr) c.*28+18863C>A (n.*28+18863C>A) c.2407C>A (p.Pro803Thr) c.1741C>A (p.Pro581Thr) | dbSNP gnomAD v4 |
| 7 | g.55191791C= | CA1708922562 | EGFR | c.2383C= (p.Pro795=) c.891C= c.2542C= (p.Pro848=) c.*28+18863C= (n.*28+18863C=) c.2407C= (p.Pro803=) c.1741C= (p.Pro581=) | |
| 7 | g.55191791C>G | CA367580207 | EGFR | c.2383C>G (p.Pro795Ala) c.891C>G c.2542C>G (p.Pro848Ala) c.*28+18863C>G (n.*28+18863C>G) c.2407C>G (p.Pro803Ala) c.1741C>G (p.Pro581Ala) | dbSNP |
| 7 | g.55191791C>T | CA367580208 | EGFR | c.2383C>T (p.Pro795Ser) c.891C>T c.2542C>T (p.Pro848Ser) c.*28+18863C>T (n.*28+18863C>T) c.2407C>T (p.Pro803Ser) c.1741C>T (p.Pro581Ser) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191792C>A | CA367580209 | EGFR | c.2384C>A (p.Pro795Gln) c.892C>A c.2543C>A (p.Pro848Gln) c.*28+18864C>A (n.*28+18864C>A) c.2408C>A (p.Pro803Gln) c.1742C>A (p.Pro581Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191792C= | CA1708922568 | EGFR | c.2384C= (p.Pro795=) c.892C= c.2543C= (p.Pro848=) c.*28+18864C= (n.*28+18864C=) c.2408C= (p.Pro803=) c.1742C= (p.Pro581=) | |
| 7 | g.55191792C>G | CA367580210 | EGFR | c.2384C>G (p.Pro795Arg) c.892C>G c.2543C>G (p.Pro848Arg) c.*28+18864C>G (n.*28+18864C>G) c.2408C>G (p.Pro803Arg) c.1742C>G (p.Pro581Arg) | dbSNP |
| 7 | g.55191792C>T | CA135927 | EGFR | c.2384C>T (p.Pro795Leu) c.892C>T c.2543C>T (p.Pro848Leu) c.*28+18864C>T (n.*28+18864C>T) c.2408C>T (p.Pro803Leu) c.1742C>T (p.Pro581Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191793G>A | CA156276 | EGFR | c.2385G>A (p.Pro795=) c.893G>A c.2544G>A (p.Pro848=) c.*28+18865G>A (n.*28+18865G>A) c.2409G>A (p.Pro803=) c.1743G>A (p.Pro581=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191793G>C | CA454965630 | EGFR | c.2385G>C (p.Pro795=) c.893G>C c.2544G>C (p.Pro848=) c.*28+18865G>C (n.*28+18865G>C) c.2409G>C (p.Pro803=) c.1743G>C (p.Pro581=) | dbSNP |
| 7 | g.55191793G= | CA1708922578 | EGFR | c.2385G= (p.Pro795=) c.893G= c.2544G= (p.Pro848=) c.*28+18865G= (n.*28+18865G=) c.2409G= (p.Pro803=) c.1743G= (p.Pro581=) | |
| 7 | g.55191793G>T | CA158934221 | EGFR | c.2385G>T (p.Pro795=) c.893G>T c.2544G>T (p.Pro848=) c.*28+18865G>T (n.*28+18865G>T) c.2409G>T (p.Pro803=) c.1743G>T (p.Pro581=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191794C>A | CA367580211 | EGFR | c.2386C>A (p.Gln796Lys) c.894C>A c.2545C>A (p.Gln849Lys) c.*28+18866C>A (n.*28+18866C>A) c.2410C>A (p.Gln804Lys) c.1744C>A (p.Gln582Lys) | dbSNP |
| 7 | g.55191794C= | CA1708922584 | EGFR | c.2386C= (p.Gln796=) c.894C= c.2545C= (p.Gln849=) c.*28+18866C= (n.*28+18866C=) c.2410C= (p.Gln804=) c.1744C= (p.Gln582=) | |
| 7 | g.55191794C>G | CA367580212 | EGFR | c.2386C>G (p.Gln796Glu) c.894C>G c.2545C>G (p.Gln849Glu) c.*28+18866C>G (n.*28+18866C>G) c.2410C>G (p.Gln804Glu) c.1744C>G (p.Gln582Glu) | dbSNP |
| 7 | g.55191794C>T | CA367580213 | EGFR | c.2386C>T (p.Gln796Ter) c.894C>T c.2545C>T (p.Gln849Ter) c.*28+18866C>T (n.*28+18866C>T) c.2410C>T (p.Gln804Ter) c.1744C>T (p.Gln582Ter) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191795A>C | CA367580216 | EGFR | c.2387A>C (p.Gln796Pro) c.895A>C c.2546A>C (p.Gln849Pro) c.*28+18867A>C (n.*28+18867A>C) c.2411A>C (p.Gln804Pro) c.1745A>C (p.Gln582Pro) | gnomAD v4 |
| 7 | g.55191795A>G | CA367580214 | EGFR | c.2387A>G (p.Gln796Arg) c.895A>G c.2546A>G (p.Gln849Arg) c.*28+18867A>G (n.*28+18867A>G) c.2411A>G (p.Gln804Arg) c.1745A>G (p.Gln582Arg) | dbSNP COSMIC |
| 7 | g.55191795A>T | CA367580215 | EGFR | c.2387A>T (p.Gln796Leu) c.895A>T c.2546A>T (p.Gln849Leu) c.*28+18867A>T (n.*28+18867A>T) c.2411A>T (p.Gln804Leu) c.1745A>T (p.Gln582Leu) | dbSNP |
| 7 | g.55191796G>A | CA454965631 | EGFR | c.2388G>A (p.Gln796=) c.896G>A c.2547G>A (p.Gln849=) c.*28+18868G>A (n.*28+18868G>A) c.2412G>A (p.Gln804=) c.1746G>A (p.Gln582=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191796G>C | CA367580217 | EGFR | c.2388G>C (p.Gln796His) c.896G>C c.2547G>C (p.Gln849His) c.*28+18868G>C (n.*28+18868G>C) c.2412G>C (p.Gln804His) c.1746G>C (p.Gln582His) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191796G= | CA1708922589 | EGFR | c.2388G= (p.Gln796=) c.896G= c.2547G= (p.Gln849=) c.*28+18868G= (n.*28+18868G=) c.2412G= (p.Gln804=) c.1746G= (p.Gln582=) | |
| 7 | g.55191796G>T | CA367580218 | EGFR | c.2388G>T (p.Gln796His) c.896G>T c.2547G>T (p.Gln849His) c.*28+18868G>T (n.*28+18868G>T) c.2412G>T (p.Gln804His) c.1746G>T (p.Gln582His) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191797C>A | CA367580219 | EGFR | c.2389C>A (p.His797Asn) c.897C>A c.2548C>A (p.His850Asn) c.*28+18869C>A (n.*28+18869C>A) c.2413C>A (p.His805Asn) c.1747C>A (p.His583Asn) | dbSNP COSMIC |
| 7 | g.55191797C>G | CA367580220 | EGFR | c.2389C>G (p.His797Asp) c.897C>G c.2548C>G (p.His850Asp) c.*28+18869C>G (n.*28+18869C>G) c.2413C>G (p.His805Asp) c.1747C>G (p.His583Asp) | dbSNP COSMIC |
| 7 | g.55191797C>T | CA367580221 | EGFR | c.2389C>T (p.His797Tyr) c.897C>T c.2548C>T (p.His850Tyr) c.*28+18869C>T (n.*28+18869C>T) c.2413C>T (p.His805Tyr) c.1747C>T (p.His583Tyr) | dbSNP COSMIC |
| 7 | g.55191798A>C | CA367580222 | EGFR | c.2390A>C (p.His797Pro) c.898A>C c.2549A>C (p.His850Pro) c.*28+18870A>C (n.*28+18870A>C) c.2414A>C (p.His805Pro) c.1748A>C (p.His583Pro) | |
| 7 | g.55191798A>G | CA367580223 | EGFR | c.2390A>G (p.His797Arg) c.898A>G c.2549A>G (p.His850Arg) c.*28+18870A>G (n.*28+18870A>G) c.2414A>G (p.His805Arg) c.1748A>G (p.His583Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191798A>T | CA367580224 | EGFR | c.2390A>T (p.His797Leu) c.898A>T c.2549A>T (p.His850Leu) c.*28+18870A>T (n.*28+18870A>T) c.2414A>T (p.His805Leu) c.1748A>T (p.His583Leu) | dbSNP gnomAD v4 |
| 7 | g.55191799T>A | CA367580225 | EGFR | c.2391T>A (p.His797Gln) c.899T>A c.2550T>A (p.His850Gln) c.*28+18871T>A (n.*28+18871T>A) c.2415T>A (p.His805Gln) c.1749T>A (p.His583Gln) | dbSNP |
| 7 | g.55191799T>C | CA454965633 | EGFR | c.2391T>C (p.His797=) c.899T>C c.2550T>C (p.His850=) c.*28+18871T>C (n.*28+18871T>C) c.2415T>C (p.His805=) c.1749T>C (p.His583=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191799T>G | CA367580226 | EGFR | c.2391T>G (p.His797Gln) c.899T>G c.2550T>G (p.His850Gln) c.*28+18871T>G (n.*28+18871T>G) c.2415T>G (p.His805Gln) c.1749T>G (p.His583Gln) | ClinVar dbSNP |
| 7 | g.55191799T= | CA1708922592 | EGFR | c.2391T= (p.His797=) c.899T= c.2550T= (p.His850=) c.*28+18871T= (n.*28+18871T=) c.2415T= (p.His805=) c.1749T= (p.His583=) | |
| 7 | g.55191800G>A | CA367580229 | EGFR | c.2392G>A (p.Val798Ile) c.899+1G>A c.2551G>A (p.Val851Ile) c.*28+18872G>A (n.*28+18872G>A) c.2416G>A (p.Val806Ile) c.1750G>A (p.Val584Ile) | dbSNP COSMIC |
| 7 | g.55191800G>C | CA367580228 | EGFR | c.2392G>C (p.Val798Leu) c.899+1G>C c.2551G>C (p.Val851Leu) c.*28+18872G>C (n.*28+18872G>C) c.2416G>C (p.Val806Leu) c.1750G>C (p.Val584Leu) | dbSNP |
| 7 | g.55191800G>T | CA367580227 | EGFR | c.2392G>T (p.Val798Phe) c.899+1G>T c.2551G>T (p.Val851Phe) c.*28+18872G>T (n.*28+18872G>T) c.2416G>T (p.Val806Phe) c.1750G>T (p.Val584Phe) | dbSNP |
| 7 | g.55191801T>A | CA367580230 | EGFR | c.2393T>A (p.Val798Asp) c.899+2T>A c.2552T>A (p.Val851Asp) c.*28+18873T>A (n.*28+18873T>A) c.2417T>A (p.Val806Asp) c.1751T>A (p.Val584Asp) | dbSNP |
| 7 | g.55191801T>C | CA367580231 | EGFR | c.2393T>C (p.Val798Ala) c.899+2T>C c.2552T>C (p.Val851Ala) c.*28+18873T>C (n.*28+18873T>C) c.2417T>C (p.Val806Ala) c.1751T>C (p.Val584Ala) | dbSNP COSMIC |
| 7 | g.55191801T>G | CA367580232 | EGFR | c.2393T>G (p.Val798Gly) c.899+2T>G c.2552T>G (p.Val851Gly) c.*28+18873T>G (n.*28+18873T>G) c.2417T>G (p.Val806Gly) c.1751T>G (p.Val584Gly) | dbSNP |
| 7 | g.55191802C>A | CA454965636 | EGFR | c.2394C>A (p.Val798=) c.899+3C>A c.2553C>A (p.Val851=) c.*28+18874C>A (n.*28+18874C>A) c.2418C>A (p.Val806=) c.1752C>A (p.Val584=) | dbSNP |
| 7 | g.55191802C>G | CA454965634 | EGFR | c.2394C>G (p.Val798=) c.899+3C>G c.2553C>G (p.Val851=) c.*28+18874C>G (n.*28+18874C>G) c.2418C>G (p.Val806=) c.1752C>G (p.Val584=) | dbSNP gnomAD v4 |
| 7 | g.55191802C>T | CA454965635 | EGFR | c.2394C>T (p.Val798=) c.899+3C>T c.2553C>T (p.Val851=) c.*28+18874C>T (n.*28+18874C>T) c.2418C>T (p.Val806=) c.1752C>T (p.Val584=) | dbSNP |
| 7 | g.55191803A>C | CA367580233 | EGFR | c.2395A>C (p.Lys799Gln) c.899+4A>C c.2554A>C (p.Lys852Gln) c.*28+18875A>C (n.*28+18875A>C) c.2419A>C (p.Lys807Gln) c.1753A>C (p.Lys585Gln) | |
| 7 | g.55191803A>G | CA367580234 | EGFR | c.2395A>G (p.Lys799Glu) c.899+4A>G c.2554A>G (p.Lys852Glu) c.*28+18875A>G (n.*28+18875A>G) c.2419A>G (p.Lys807Glu) c.1753A>G (p.Lys585Glu) | dbSNP |
| 7 | g.55191803A>T | CA367580235 | EGFR | c.2395A>T (p.Lys799Ter) c.899+4A>T c.2554A>T (p.Lys852Ter) c.*28+18875A>T (n.*28+18875A>T) c.2419A>T (p.Lys807Ter) c.1753A>T (p.Lys585Ter) | dbSNP |
| 7 | g.55191804A= | CA1708922595 | EGFR | c.2396A= (p.Lys799=) c.899+5A= c.2555A= (p.Lys852=) c.*28+18876A= (n.*28+18876A=) c.2420A= (p.Lys807=) c.1754A= (p.Lys585=) | |
| 7 | g.55191804A>C | CA367580236 | EGFR | c.2396A>C (p.Lys799Thr) c.899+5A>C c.2555A>C (p.Lys852Thr) c.*28+18876A>C (n.*28+18876A>C) c.2420A>C (p.Lys807Thr) c.1754A>C (p.Lys585Thr) | |
| 7 | g.55191804A>G | CA367580237 | EGFR | c.2396A>G (p.Lys799Arg) c.899+5A>G c.2555A>G (p.Lys852Arg) c.*28+18876A>G (n.*28+18876A>G) c.2420A>G (p.Lys807Arg) c.1754A>G (p.Lys585Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191804A>T | CA367580238 | EGFR | c.2396A>T (p.Lys799Met) c.899+5A>T c.2555A>T (p.Lys852Met) c.*28+18876A>T (n.*28+18876A>T) c.2420A>T (p.Lys807Met) c.1754A>T (p.Lys585Met) | dbSNP |
| 7 | g.55191805G>A | CA454965637 | EGFR | c.2397G>A (p.Lys799=) c.899+6G>A c.2556G>A (p.Lys852=) c.*28+18877G>A (n.*28+18877G>A) c.2421G>A (p.Lys807=) c.1755G>A (p.Lys585=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191805G>C | CA367580239 | EGFR | c.2397G>C (p.Lys799Asn) c.899+6G>C c.2556G>C (p.Lys852Asn) c.*28+18877G>C (n.*28+18877G>C) c.2421G>C (p.Lys807Asn) c.1755G>C (p.Lys585Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191805G= | CA1708922599 | EGFR | c.2397G= (p.Lys799=) c.899+6G= c.2556G= (p.Lys852=) c.*28+18877G= (n.*28+18877G=) c.2421G= (p.Lys807=) c.1755G= (p.Lys585=) | |
| 7 | g.55191805G>T | CA367580240 | EGFR | c.2397G>T (p.Lys799Asn) c.899+6G>T c.2556G>T (p.Lys852Asn) c.*28+18877G>T (n.*28+18877G>T) c.2421G>T (p.Lys807Asn) c.1755G>T (p.Lys585Asn) | dbSNP COSMIC |
| 7 | g.55191806A>C | CA367580243 | EGFR | c.2398A>C (p.Ile800Leu) c.899+7A>C c.2557A>C (p.Ile853Leu) c.*28+18878A>C (n.*28+18878A>C) c.2422A>C (p.Ile808Leu) c.1756A>C (p.Ile586Leu) | dbSNP |
| 7 | g.55191806A>G | CA367580242 | EGFR | c.2398A>G (p.Ile800Val) c.899+7A>G c.2557A>G (p.Ile853Val) c.*28+18878A>G (n.*28+18878A>G) c.2422A>G (p.Ile808Val) c.1756A>G (p.Ile586Val) | |
| 7 | g.55191806A>T | CA367580241 | EGFR | c.2398A>T (p.Ile800Phe) c.899+7A>T c.2557A>T (p.Ile853Phe) c.*28+18878A>T (n.*28+18878A>T) c.2422A>T (p.Ile808Phe) c.1756A>T (p.Ile586Phe) | |
| 7 | g.55191807T>A | CA367580244 | EGFR | c.2399T>A (p.Ile800Asn) c.899+8T>A c.2558T>A (p.Ile853Asn) c.*28+18879T>A (n.*28+18879T>A) c.2423T>A (p.Ile808Asn) c.1757T>A (p.Ile586Asn) | dbSNP |
| 7 | g.55191807T>C | CA367580245 | EGFR | c.2399T>C (p.Ile800Thr) c.899+8T>C c.2558T>C (p.Ile853Thr) c.*28+18879T>C (n.*28+18879T>C) c.2423T>C (p.Ile808Thr) c.1757T>C (p.Ile586Thr) | COSMIC |
| 7 | g.55191807T>G | CA367580246 | EGFR | c.2399T>G (p.Ile800Ser) c.899+8T>G c.2558T>G (p.Ile853Ser) c.*28+18879T>G (n.*28+18879T>G) c.2423T>G (p.Ile808Ser) c.1757T>G (p.Ile586Ser) | dbSNP |
| 7 | g.55191808C>A | CA454965638 | EGFR | c.2400C>A (p.Ile800=) c.899+9C>A c.2559C>A (p.Ile853=) c.*28+18880C>A (n.*28+18880C>A) c.2424C>A (p.Ile808=) c.1758C>A (p.Ile586=) | dbSNP gnomAD v4 |
| 7 | g.55191808C>G | CA367580247 | EGFR | c.2400C>G (p.Ile800Met) c.899+9C>G c.2559C>G (p.Ile853Met) c.*28+18880C>G (n.*28+18880C>G) c.2424C>G (p.Ile808Met) c.1758C>G (p.Ile586Met) | dbSNP |
| 7 | g.55191808C>T | CA454965640 | EGFR | c.2400C>T (p.Ile800=) c.899+9C>T c.2559C>T (p.Ile853=) c.*28+18880C>T (n.*28+18880C>T) c.2424C>T (p.Ile808=) c.1758C>T (p.Ile586=) | dbSNP COSMIC |
| 7 | g.55191809A= | CA1708922602 | EGFR | c.2401A= (p.Thr801=) c.899+10A= c.2560A= (p.Thr854=) c.*28+18881A= (n.*28+18881A=) c.2425A= (p.Thr809=) c.1759A= (p.Thr587=) | |
| 7 | g.55191809A>C | CA367580248 | EGFR | c.2401A>C (p.Thr801Pro) c.899+10A>C c.2560A>C (p.Thr854Pro) c.*28+18881A>C (n.*28+18881A>C) c.2425A>C (p.Thr809Pro) c.1759A>C (p.Thr587Pro) | dbSNP COSMIC |
| 7 | g.55191809A>G | CA367580249 | EGFR | c.2401A>G (p.Thr801Ala) c.899+10A>G c.2560A>G (p.Thr854Ala) c.*28+18881A>G (n.*28+18881A>G) c.2425A>G (p.Thr809Ala) c.1759A>G (p.Thr587Ala) | ClinVar dbSNP COSMIC |
| 7 | g.55191809A>T | CA367580250 | EGFR | c.2401A>T (p.Thr801Ser) c.899+10A>T c.2560A>T (p.Thr854Ser) c.*28+18881A>T (n.*28+18881A>T) c.2425A>T (p.Thr809Ser) c.1759A>T (p.Thr587Ser) | dbSNP COSMIC |
| 7 | g.55191810C>A | CA367580251 | EGFR | c.2402C>A (p.Thr801Lys) c.899+11C>A c.2561C>A (p.Thr854Lys) c.*28+18882C>A (n.*28+18882C>A) c.2426C>A (p.Thr809Lys) c.1760C>A (p.Thr587Lys) | dbSNP |
| 7 | g.55191810C>G | CA367580252 | EGFR | c.2402C>G (p.Thr801Arg) c.899+11C>G c.2561C>G (p.Thr854Arg) c.*28+18882C>G (n.*28+18882C>G) c.2426C>G (p.Thr809Arg) c.1760C>G (p.Thr587Arg) | dbSNP |
| 7 | g.55191810C>T | CA367580253 | EGFR | c.2402C>T (p.Thr801Ile) c.899+11C>T c.2561C>T (p.Thr854Ile) c.*28+18882C>T (n.*28+18882C>T) c.2426C>T (p.Thr809Ile) c.1760C>T (p.Thr587Ile) | ClinVar dbSNP COSMIC |
| 7 | g.55191811A>C | CA454965641 | EGFR | c.2403A>C (p.Thr801=) c.899+12A>C c.2562A>C (p.Thr854=) c.*28+18883A>C (n.*28+18883A>C) c.2427A>C (p.Thr809=) c.1761A>C (p.Thr587=) | |
| 7 | g.55191811A>G | CA454965642 | EGFR | c.2403A>G (p.Thr801=) c.899+12A>G c.2562A>G (p.Thr854=) c.*28+18883A>G (n.*28+18883A>G) c.2427A>G (p.Thr809=) c.1761A>G (p.Thr587=) | |
| 7 | g.55191811A>T | CA454965643 | EGFR | c.2403A>T (p.Thr801=) c.899+12A>T c.2562A>T (p.Thr854=) c.*28+18883A>T (n.*28+18883A>T) c.2427A>T (p.Thr809=) c.1761A>T (p.Thr587=) | dbSNP |
| 7 | g.55191812G>A | CA367580254 | EGFR | c.2404G>A (p.Asp802Asn) c.899+13G>A c.2563G>A (p.Asp855Asn) c.*28+18884G>A (n.*28+18884G>A) c.2428G>A (p.Asp810Asn) c.1762G>A (p.Asp588Asn) | dbSNP COSMIC |
| 7 | g.55191812G>C | CA367580255 | EGFR | c.2404G>C (p.Asp802His) c.899+13G>C c.2563G>C (p.Asp855His) c.*28+18884G>C (n.*28+18884G>C) c.2428G>C (p.Asp810His) c.1762G>C (p.Asp588His) | dbSNP |
| 7 | g.55191812G>T | CA367580256 | EGFR | c.2404G>T (p.Asp802Tyr) c.899+13G>T c.2563G>T (p.Asp855Tyr) c.*28+18884G>T (n.*28+18884G>T) c.2428G>T (p.Asp810Tyr) c.1762G>T (p.Asp588Tyr) | |
| 7 | g.55191813A>C | CA367580258 | EGFR | c.2405A>C (p.Asp802Ala) c.899+14A>C c.2564A>C (p.Asp855Ala) c.*28+18885A>C (n.*28+18885A>C) c.2429A>C (p.Asp810Ala) c.1763A>C (p.Asp588Ala) | |
| 7 | g.55191813A>G | CA367580259 | EGFR | c.2405A>G (p.Asp802Gly) c.899+14A>G c.2564A>G (p.Asp855Gly) c.*28+18885A>G (n.*28+18885A>G) c.2429A>G (p.Asp810Gly) c.1763A>G (p.Asp588Gly) | COSMIC |
| 7 | g.55191813A>T | CA367580257 | EGFR | c.2405A>T (p.Asp802Val) c.899+14A>T c.2564A>T (p.Asp855Val) c.*28+18885A>T (n.*28+18885A>T) c.2429A>T (p.Asp810Val) c.1763A>T (p.Asp588Val) |