Primary Site >> Stomach Cancer
Gene >> GPR37
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764741:124764741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.236C>T |
| AA Mutation | p.Ala79Val(p.A79V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764436:124764436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.541T>A |
| AA Mutation | p.Tyr181Asn(p.Y181N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764702:124764702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275C>T |
| AA Mutation | p.Pro92Leu(p.P92L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764420:124764420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.557C>T |
| AA Mutation | p.Ala186Val(p.A186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764100:124764100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877C>T |
| AA Mutation | p.Arg293Trp(p.R293W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124746976:124746976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391T>C |
| AA Mutation | p.Val464Ala(p.V464A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764246:124764246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.731G>A |
| AA Mutation | p.Arg244His(p.R244H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124747165:124747165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369674783 |
| CDS Mutation | c.1202G>A |
| AA Mutation | p.Arg401His(p.R401H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764000:124764000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977A>G |
| AA Mutation | p.Lys326Arg(p.K326R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124747237:124747237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1130C>A |
| AA Mutation | p.Ser377Tyr(p.S377Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303921 |
| Start | 124746629:124746629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1738A>C |
| AA Mutation | p.Ser580Arg(p.S580R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764689:124764689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.288G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764188:124764188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303921 |
| Start | 124747020:124747020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1347T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303921 |
| Start | 124747053:124747053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368914982 |
| CDS Mutation | c.1314C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000303921 |
| Start | 124764436:124764436(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.541delT |
| AA Mutation | p.Tyr181ThrfsTer65(p.Y181Tfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |