Primary Site >> Stomach Cancer
Gene >> ADCY2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000338316 |
| Start | 7520897:7520897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568C>A |
| AA Mutation | p.Gln190Lys(p.Q190K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7695771:7695771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.889G>A |
| AA Mutation | p.Val297Ile(p.V297I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7706826:7706826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1192C>A |
| AA Mutation | p.Leu398Met(p.L398M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7520864:7520864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Ala179Thr(p.A179T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7709221:7709221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141886153 |
| CDS Mutation | c.1412G>A |
| AA Mutation | p.Arg471Gln(p.R471Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7690823:7690823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Trp(p.R285W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7772948:7772948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2231G>A |
| AA Mutation | p.Cys744Tyr(p.C744Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7727168:7727168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762541068 |
| CDS Mutation | c.1778G>A |
| AA Mutation | p.Arg593Gln(p.R593Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7766741:7766741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768691352 |
| CDS Mutation | c.2149A>G |
| AA Mutation | p.Thr717Ala(p.T717A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7698332:7698332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1067A>G |
| AA Mutation | p.Lys356Arg(p.K356R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7698332:7698332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1067A>C |
| AA Mutation | p.Lys356Thr(p.K356T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7414726:7414726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.364T>C |
| AA Mutation | p.Tyr122His(p.Y122H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7690749:7690749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.779T>C |
| AA Mutation | p.Ile260Thr(p.I260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7826783:7826783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3188T>C |
| AA Mutation | p.Ile1063Thr(p.I1063T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7802251:7802251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2662G>A |
| AA Mutation | p.Val888Ile(p.V888I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7709223:7709223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1414A>G |
| AA Mutation | p.Ser472Gly(p.S472G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7820682:7820682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3116A>G |
| AA Mutation | p.Lys1039Arg(p.K1039R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7804613:7804613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2804T>G |
| AA Mutation | p.Val935Gly(p.V935G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7820672:7820672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3106G>T |
| AA Mutation | p.Val1036Phe(p.V1036F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338316 |
| Start | 7396430:7396430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.134C>T |
| AA Mutation | p.Pro45Leu(p.P45L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7396452:7396452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7707721:7707721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1284T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7802244:7802244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2655C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7789662:7789662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2490A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7789731:7789731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760993821 |
| CDS Mutation | c.2559C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7414656:7414656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758065979 |
| CDS Mutation | c.294C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7396368:7396368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530639895 |
| CDS Mutation | c.72C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7709324:7709324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1515G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7709369:7709369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761978082 |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7789746:7789746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370476148 |
| CDS Mutation | c.2574C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7626247:7626247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.651G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7626283:7626283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149422716 |
| CDS Mutation | c.687G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338316 |
| Start | 7707748:7707748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112493968 |
| CDS Mutation | c.1311C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |