Primary Site >> Stomach Cancer
Gene >> TRPM2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44364244:44364244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759790819 |
| CDS Mutation | c.385G>A |
| AA Mutation | p.Asp129Asn(p.D129N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44379099:44379099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1117G>A |
| AA Mutation | p.Asp373Asn(p.D373N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44405919:44405919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369200126 |
| CDS Mutation | c.2672C>T |
| AA Mutation | p.Thr891Met(p.T891M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44399325:44399325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150593294 |
| CDS Mutation | c.2092G>A |
| AA Mutation | p.Glu698Lys(p.E698K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44406612:44406612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2809T>C |
| AA Mutation | p.Phe937Leu(p.F937L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44418040:44418040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3260T>G |
| AA Mutation | p.Leu1087Arg(p.L1087R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44406616:44406616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2813T>G |
| AA Mutation | p.Leu938Arg(p.L938R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44427065:44427065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144290883 |
| CDS Mutation | c.3928C>T |
| AA Mutation | p.Arg1310Cys(p.R1310C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44391013:44391013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1428G>C |
| AA Mutation | p.Glu476Asp(p.E476D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44405241:44405241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774923547 |
| CDS Mutation | c.2638G>A |
| AA Mutation | p.Val880Met(p.V880M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44401805:44401805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747955952 |
| CDS Mutation | c.2446G>A |
| AA Mutation | p.Val816Met(p.V816M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000300482 |
| Start | 44418555:44418555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755543384 |
| CDS Mutation | c.3461A>C |
| AA Mutation | p.Lys1154Thr(p.K1154T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44414002:44414002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138586774 |
| CDS Mutation | c.3074C>T |
| AA Mutation | p.Thr1025Met(p.T1025M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300482 |
| Start | 44390975:44390975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755444540 |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Arg464Cys(p.R464C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44413931:44413931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768276564 |
| CDS Mutation | c.3003C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44413907:44413907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199995128 |
| CDS Mutation | c.2979G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44395467:44395467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1848C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44391349:44391349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752773465 |
| CDS Mutation | c.1518C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44379008:44379008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747609422 |
| CDS Mutation | c.1026C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44400363:44400363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2313C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44391385:44391385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1554C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44391400:44391400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747647717 |
| CDS Mutation | c.1569C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44413955:44413955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3027C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44418520:44418520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3426G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300482 |
| Start | 44366819:44366819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300482 |
| Start | 44366853:44366853(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776641072 |
| CDS Mutation | c.529delG |
| AA Mutation | p.Ala177ProfsTer6(p.A177Pfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300482 |
| Start | 44391412:44391412(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1584delC |
| AA Mutation | p.Ser529ProfsTer74(p.S529Pfs*74) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |