Primary Site >> Stomach Cancer
Gene >> ARHGEF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41894481:41894481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775G>T |
| AA Mutation | p.Ala259Ser(p.A259S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41902653:41902653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1618G>A |
| AA Mutation | p.Val540Met(p.V540M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41906487:41906487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375950739 |
| CDS Mutation | c.2522C>T |
| AA Mutation | p.Ala841Val(p.A841V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41898564:41898564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1244T>C |
| AA Mutation | p.Val415Ala(p.V415A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41903318:41903318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1750G>A |
| AA Mutation | p.Glu584Lys(p.E584K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41893293:41893293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Glu212Lys(p.E212K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41902800:41902800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1640C>T |
| AA Mutation | p.Pro547Leu(p.P547L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41895424:41895424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.953G>T |
| AA Mutation | p.Gly318Val(p.G318V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41895396:41895396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925T>C |
| AA Mutation | p.Ser309Pro(p.S309P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354532 |
| Start | 41905234:41905234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781883859 |
| CDS Mutation | c.2309G>A |
| AA Mutation | p.Arg770His(p.R770H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354532 |
| Start | 41901912:41901912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377396950 |
| CDS Mutation | c.1293C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000354532 |
| Start | 41892336:41892336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782791739 |
| CDS Mutation | c.330C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |