Primary Site >> Stomach Cancer
Gene >> ICAM5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294303:10294303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1975G>A |
| AA Mutation | p.Val659Ile(p.V659I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10293205:10293205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1424A>T |
| AA Mutation | p.Asp475Val(p.D475V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294118:10294118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1790A>G |
| AA Mutation | p.Glu597Gly(p.E597G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294049:10294049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1721G>T |
| AA Mutation | p.Arg574Met(p.R574M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10292235:10292235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.874G>A |
| AA Mutation | p.Ala292Thr(p.A292T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10292812:10292812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1162G>A |
| AA Mutation | p.Asp388Asn(p.D388N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10292258:10292258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.897G>T |
| AA Mutation | p.Gln299His(p.Q299H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10292260:10292260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.899T>C |
| AA Mutation | p.Leu300Pro(p.L300P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10293883:10293883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1651C>T |
| AA Mutation | p.Arg551Cys(p.R551C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294267:10294267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1939G>A |
| AA Mutation | p.Ala647Thr(p.A647T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10291633:10291633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.497G>T |
| AA Mutation | p.Arg166Leu(p.R166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294443:10294443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2033C>T |
| AA Mutation | p.Thr678Met(p.T678M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10291117:10291117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.128C>T |
| AA Mutation | p.Ala43Val(p.A43V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294313:10294313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1985C>T |
| AA Mutation | p.Ala662Val(p.A662V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221980 |
| Start | 10294468:10294468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758505262 |
| CDS Mutation | c.2058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |