Primary Site >> Stomach Cancer
Gene >> TGM3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2332250:2332250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1582G>T |
| AA Mutation | p.Gly528Cys(p.G528C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2309705:2309705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143797112 |
| CDS Mutation | c.56C>T |
| AA Mutation | p.Ala19Val(p.A19V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2317095:2317095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Leu233Phe(p.L233F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2328314:2328314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1282G>C |
| AA Mutation | p.Val428Leu(p.V428L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2311049:2311049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.460G>A |
| AA Mutation | p.Glu154Lys(p.E154K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2317481:2317481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370121854 |
| CDS Mutation | c.979G>A |
| AA Mutation | p.Val327Ile(p.V327I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2309677:2309677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.28A>G |
| AA Mutation | p.Asn10Asp(p.N10D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2335167:2335167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694A>G |
| AA Mutation | p.Lys565Arg(p.K565R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2317355:2317355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200047268 |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Trp(p.R285W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2317416:2317416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562802461 |
| CDS Mutation | c.914G>A |
| AA Mutation | p.Arg305Gln(p.R305Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000381458 |
| Start | 2310324:2310324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139117716 |
| CDS Mutation | c.328C>T |
| AA Mutation | p.Arg110Trp(p.R110W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2328343:2328343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540980778 |
| CDS Mutation | c.1311G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2313008:2313008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2335261:2335261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1788C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2328337:2328337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776078400 |
| CDS Mutation | c.1305C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2340506:2340506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745980148 |
| CDS Mutation | c.2007G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000381458 |
| Start | 2340443:2340443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1944C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000381458 |
| Start | 2332019:2332019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779702016 |
| CDS Mutation | c.1351C>T |
| AA Mutation | p.Gln451Ter(p.Q451*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000381458 |
| Start | 2332028:2332029(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1364dupA |
| AA Mutation | p.Ala456GlyfsTer6(p.A456Gfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |