Primary Site >> Stomach Cancer
Gene >> MMRN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935940:89935940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2260A>G |
| AA Mutation | p.Thr754Ala(p.T754A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89927900:89927900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1061A>C |
| AA Mutation | p.Asn354Thr(p.N354T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935863:89935863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2183T>C |
| AA Mutation | p.Leu728Pro(p.L728P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89909313:89909313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661A>G |
| AA Mutation | p.Thr221Ala(p.T221A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935452:89935452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1772A>G |
| AA Mutation | p.Glu591Gly(p.E591G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935553:89935553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1873C>A |
| AA Mutation | p.Leu625Ile(p.L625I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89927800:89927800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201813411 |
| CDS Mutation | c.961A>T |
| AA Mutation | p.Met321Leu(p.M321L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895218:89895218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.247C>A |
| AA Mutation | p.Leu83Met(p.L83M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89953185:89953185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536978530 |
| CDS Mutation | c.3454G>A |
| AA Mutation | p.Glu1152Lys(p.E1152K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89953269:89953269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3538G>A |
| AA Mutation | p.Glu1180Lys(p.E1180K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935565:89935565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1885G>C |
| AA Mutation | p.Asp629His(p.D629H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89951625:89951625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368250909 |
| CDS Mutation | c.3139C>T |
| AA Mutation | p.Arg1047Trp(p.R1047W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89909357:89909357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.705A>C |
| AA Mutation | p.Lys235Asn(p.K235N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89953054:89953054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764291894 |
| CDS Mutation | c.3323C>T |
| AA Mutation | p.Thr1108Met(p.T1108M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935431:89935431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1751A>G |
| AA Mutation | p.Glu584Gly(p.E584G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895159:89895159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188C>T |
| AA Mutation | p.Ala63Val(p.A63V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895061:89895061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935108:89935108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1428G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89895022:89895022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.51C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89936647:89936647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762745325 |
| CDS Mutation | c.2967G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89927862:89927862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1023G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935075:89935075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138127460 |
| CDS Mutation | c.1395T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264790 |
| Start | 89953038:89953038(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3312delT |
| AA Mutation | p.Phe1104LeufsTer8(p.F1104Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264790 |
| Start | 89895128:89895128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Gln53Ter(p.Q53*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264790 |
| Start | 89935098:89935099(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1418_1419insTATGTCTCTT |
| AA Mutation | p.Cys474MetfsTer5(p.C474Mfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |