Primary Site >> Stomach Cancer
Gene >> NEUROD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678430:181678430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.431G>A |
| AA Mutation | p.Arg144His(p.R144H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181677918:181677918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Gly315Arg(p.G315R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678568:181678568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293G>A |
| AA Mutation | p.Arg98His(p.R98H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678608:181678608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Gly85Ser(p.G85S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678607:181678607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.254G>A |
| AA Mutation | p.Gly85Asp(p.G85D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678227:181678227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Ala212Thr(p.A212T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181677937:181677937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.924G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678222:181678222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.639C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678306:181678306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538415264 |
| CDS Mutation | c.555G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678813:181678813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188971339 |
| CDS Mutation | c.48C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678720:181678720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.141C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678120:181678120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.741C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181678849:181678849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295108 |
| Start | 181677994:181677994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780843075 |
| CDS Mutation | c.867G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |