Primary Site >> Stomach Cancer
Gene >> MCAM
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264036 |
| Start | 119312267:119312267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1023C>G |
| AA Mutation | p.Asn341Lys(p.N341K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119311876:119311876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755944376 |
| CDS Mutation | c.1217G>A |
| AA Mutation | p.Arg406His(p.R406H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119311847:119311847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199820957 |
| CDS Mutation | c.1246G>A |
| AA Mutation | p.Gly416Ser(p.G416S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119314898:119314898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747992430 |
| CDS Mutation | c.335G>A |
| AA Mutation | p.Arg112His(p.R112H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119314875:119314875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358C>T |
| AA Mutation | p.Arg120Cys(p.R120C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119312588:119312588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369044315 |
| CDS Mutation | c.800G>A |
| AA Mutation | p.Arg267His(p.R267H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264036 |
| Start | 119314987:119314987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.246G>C |
| AA Mutation | p.Gln82His(p.Q82H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264036 |
| Start | 119312900:119312900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264036 |
| Start | 119312384:119312384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264036 |
| Start | 119314903:119314903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770425833 |
| CDS Mutation | c.330C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264036 |
| Start | 119314907:119314908(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.325dupC |
| AA Mutation | p.Gln109ProfsTer45(p.Q109Pfs*45) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264036 |
| Start | 119311644:119311645(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1292dupC |
| AA Mutation | p.Trp432LeufsTer22(p.W432Lfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |