Primary Site >> Stomach Cancer
Gene >> LTBP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74555638:74555638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.886C>A |
| AA Mutation | p.Arg296Ser(p.R296S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74508707:74508707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3549G>T |
| AA Mutation | p.Glu1183Asp(p.E1183D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74585920:74585920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.764G>T |
| AA Mutation | p.Gly255Val(p.G255V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74502905:74502905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760591150 |
| CDS Mutation | c.4918C>T |
| AA Mutation | p.Arg1640Cys(p.R1640C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74552979:74552979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105T>C |
| AA Mutation | p.Cys369Arg(p.C369R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74506809:74506809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371669746 |
| CDS Mutation | c.3922G>A |
| AA Mutation | p.Ala1308Thr(p.A1308T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74501444:74501444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371338219 |
| CDS Mutation | c.5317G>A |
| AA Mutation | p.Val1773Ile(p.V1773I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74501510:74501510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149242944 |
| CDS Mutation | c.5251G>A |
| AA Mutation | p.Val1751Met(p.V1751M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74507257:74507257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3829G>A |
| AA Mutation | p.Glu1277Lys(p.E1277K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74509791:74509791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375244685 |
| CDS Mutation | c.3220G>A |
| AA Mutation | p.Ala1074Thr(p.A1074T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74508645:74508645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45468895 |
| CDS Mutation | c.3611C>T |
| AA Mutation | p.Ala1204Val(p.A1204V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74502841:74502841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4982C>T |
| AA Mutation | p.Pro1661Leu(p.P1661L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74532441:74532441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs180947562 |
| CDS Mutation | c.1972C>T |
| AA Mutation | p.Arg658Trp(p.R658W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261978 |
| Start | 74585935:74585935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.749G>A |
| AA Mutation | p.Ser250Asn(p.S250N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74506762:74506762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3969T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74528520:74528520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772586463 |
| CDS Mutation | c.2331G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74502882:74502882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199805158 |
| CDS Mutation | c.4941C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74528619:74528619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150924217 |
| CDS Mutation | c.2232C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74611627:74611627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.318G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74511318:74511318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201739640 |
| CDS Mutation | c.2955C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74504014:74504014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756171656 |
| CDS Mutation | c.4494G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74528968:74528968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2142G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74532442:74532442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754925929 |
| CDS Mutation | c.1971G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74611810:74611810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.135G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74508855:74508855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3501G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74611459:74611459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.486G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74611609:74611609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74555585:74555585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141536587 |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74528646:74528646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144915925 |
| CDS Mutation | c.2205C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74552329:74552329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150977144 |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261978 |
| Start | 74535993:74535993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144293300 |
| CDS Mutation | c.1797G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261978 |
| Start | 74505128:74505128(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4224delC |
| AA Mutation | p.Thr1409ProfsTer82(p.T1409Pfs*82) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261978 |
| Start | 74500904:74500904(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5446delC |
| AA Mutation | p.His1816ThrfsTer32(p.H1816Tfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261978 |
| Start | 74551215:74551215(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1535delC |
| AA Mutation | p.Pro512ArgfsTer45(p.P512Rfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261978 |
| Start | 74549896:74549896(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776807257 |
| CDS Mutation | c.1756delG |
| AA Mutation | p.Val586Ter(p.V586*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261978 |
| Start | 74555506:74555507(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1017dupC |
| AA Mutation | p.Trp340LeufsTer35(p.W340Lfs*35) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |