Primary Site >> Stomach Cancer
Gene >> EGFR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55171207:55171207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571064657 |
| CDS Mutation | c.1913C>T |
| AA Mutation | p.Thr638Met(p.T638M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55152588:55152588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759106015 |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224His(p.R224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55152632:55152632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Gly239Ser(p.G239S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55154018:55154018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760101437 |
| CDS Mutation | c.755G>A |
| AA Mutation | p.Arg252His(p.R252H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55172994:55172994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770443325 |
| CDS Mutation | c.1931C>T |
| AA Mutation | p.Pro644Leu(p.P644L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55156577:55156577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767790289 |
| CDS Mutation | c.1051A>G |
| AA Mutation | p.Ile351Val(p.I351V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55205437:55205437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3453C>A |
| AA Mutation | p.Phe1151Leu(p.F1151L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55198825:55198825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2810C>T |
| AA Mutation | p.Pro937Leu(p.P937L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55143317:55143317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Val85Met(p.V85M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55198773:55198773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2758G>T |
| AA Mutation | p.Ala920Ser(p.A920S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55155911:55155911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758748662 |
| CDS Mutation | c.971G>A |
| AA Mutation | p.Arg324His(p.R324H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275493 |
| Start | 55157744:55157744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1289C>T |
| AA Mutation | p.Thr430Ile(p.T430I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55171187:55171187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1893A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55156537:55156537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1011T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55173001:55173001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760450694 |
| CDS Mutation | c.1938C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55019337:55019337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.60G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55165297:55165297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1740C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55156816:55156816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55161554:55161554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142429250 |
| CDS Mutation | c.1554G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275493 |
| Start | 55152655:55152655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772130986 |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000275493 |
| Start | 55154055:55154055(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.797delC |
| AA Mutation | p.Pro266HisfsTer14(p.P266Hfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000275493 |
| Start | 55161591:55161591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1591C>T |
| AA Mutation | p.Arg531Ter(p.R531*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000275493 |
| Start | 55202556:55202556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749783044 |
| CDS Mutation | c.3202C>T |
| AA Mutation | p.Arg1068Ter(p.R1068*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |