Primary Site >> Stomach Cancer
Gene >> IHH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055796:219055796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142245478 |
| CDS Mutation | c.647C>T |
| AA Mutation | p.Ala216Val(p.A216V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219057613:219057613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.397T>C |
| AA Mutation | p.Trp133Arg(p.W133R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055592:219055592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Thr284Met(p.T284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055844:219055844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200082799 |
| CDS Mutation | c.599C>T |
| AA Mutation | p.Thr200Met(p.T200M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055305:219055305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773814022 |
| CDS Mutation | c.1138G>A |
| AA Mutation | p.Gly380Ser(p.G380S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055811:219055811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200898513 |
| CDS Mutation | c.632G>A |
| AA Mutation | p.Arg211His(p.R211H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055697:219055697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778096124 |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Arg249His(p.R249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295731 |
| Start | 219060345:219060345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.123A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295731 |
| Start | 219055777:219055777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374289916 |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |