Primary Site >> Stomach Cancer
Gene >> ITIH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449956 |
| Start | 52799447:52799447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.865A>G |
| AA Mutation | p.Ile289Val(p.I289V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000449956 |
| Start | 52804728:52804728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1867G>A |
| AA Mutation | p.Ala623Thr(p.A623T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449956 |
| Start | 52805822:52805822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888C>A |
| AA Mutation | p.Pro630Thr(p.P630T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449956 |
| Start | 52806990:52806990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2146G>A |
| AA Mutation | p.Ala716Thr(p.A716T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449956 |
| Start | 52803862:52803862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548417682 |
| CDS Mutation | c.1717G>A |
| AA Mutation | p.Ala573Thr(p.A573T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449956 |
| Start | 52806383:52806383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747148462 |
| CDS Mutation | c.2033G>A |
| AA Mutation | p.Arg678His(p.R678H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449956 |
| Start | 52802747:52802747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780479825 |
| CDS Mutation | c.1650C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449956 |
| Start | 52801017:52801017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1254C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449956 |
| Start | 52797885:52797885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368383671 |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |