Primary Site >> Stomach Cancer
Gene >> ELFN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373212:37373212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2323C>T |
| AA Mutation | p.Pro775Ser(p.P775S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37375179:37375179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.356C>T |
| AA Mutation | p.Thr119Met(p.T119M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374313:37374313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1222A>G |
| AA Mutation | p.Met408Val(p.M408V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373355:37373355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2180G>A |
| AA Mutation | p.Arg727His(p.R727H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373164:37373164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749366380 |
| CDS Mutation | c.2371G>A |
| AA Mutation | p.Ala791Thr(p.A791T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373727:37373727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755348427 |
| CDS Mutation | c.1808C>T |
| AA Mutation | p.Ser603Leu(p.S603L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374681:37374681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548410357 |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Pro285Leu(p.P285L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37375086:37375086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.449G>A |
| AA Mutation | p.Cys150Tyr(p.C150Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374309:37374309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1226T>C |
| AA Mutation | p.Val409Ala(p.V409A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374900:37374900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.635G>A |
| AA Mutation | p.Arg212His(p.R212H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374442:37374442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1093C>T |
| AA Mutation | p.Arg365Cys(p.R365C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373839:37373839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544695745 |
| CDS Mutation | c.1696G>A |
| AA Mutation | p.Gly566Ser(p.G566S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37375470:37375470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.65C>G |
| AA Mutation | p.Ala22Gly(p.A22G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373172:37373172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2363C>T |
| AA Mutation | p.Ala788Val(p.A788V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373946:37373946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764581745 |
| CDS Mutation | c.1589C>T |
| AA Mutation | p.Ser530Leu(p.S530L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374429:37374429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202156863 |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Arg369His(p.R369H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374799:37374799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568588590 |
| CDS Mutation | c.736C>T |
| AA Mutation | p.Arg246Trp(p.R246W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373669:37373669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1866G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37375025:37375025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.510C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374881:37374881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149082389 |
| CDS Mutation | c.654G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373237:37373237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756462935 |
| CDS Mutation | c.2298G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374200:37374200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1335T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37374920:37374920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201872308 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373618:37373618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1917C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37375385:37375385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754962894 |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373819:37373819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138855230 |
| CDS Mutation | c.1716C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402918 |
| Start | 37373639:37373639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766332484 |
| CDS Mutation | c.1896G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |