Primary Site >> Stomach Cancer
Gene >> APC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840512:112840512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373440614 |
| CDS Mutation | c.4918C>T |
| AA Mutation | p.Arg1640Trp(p.R1640W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112828865:112828865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1636A>G |
| AA Mutation | p.Ser546Gly(p.S546G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838161:112838161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757164742 |
| CDS Mutation | c.2567G>A |
| AA Mutation | p.Arg856His(p.R856H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112842160:112842160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6566A>G |
| AA Mutation | p.Lys2189Arg(p.K2189R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112801324:112801324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762117133 |
| CDS Mutation | c.775C>T |
| AA Mutation | p.Arg259Trp(p.R259W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112843137:112843137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554356011 |
| CDS Mutation | c.7543A>G |
| AA Mutation | p.Ile2515Val(p.I2515V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112841353:112841353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587780599 |
| CDS Mutation | c.5759G>A |
| AA Mutation | p.Arg1920Gln(p.R1920Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112837924:112837924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2330A>G |
| AA Mutation | p.Asp777Gly(p.D777G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840281:112840281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4687C>A |
| AA Mutation | p.Leu1563Ile(p.L1563I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112843243:112843243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7649A>T |
| AA Mutation | p.Glu2550Val(p.E2550V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112843744:112843744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8150G>C |
| AA Mutation | p.Gly2717Ala(p.G2717A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838198:112838198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2604A>C |
| AA Mutation | p.Glu868Asp(p.E868D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112839453:112839453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3859A>C |
| AA Mutation | p.Ile1287Leu(p.I1287L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112843108:112843108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147549623 |
| CDS Mutation | c.7514G>A |
| AA Mutation | p.Arg2505Gln(p.R2505Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112842514:112842514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6920C>T |
| AA Mutation | p.Ser2307Leu(p.S2307L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838908:112838908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548176472 |
| CDS Mutation | c.3314G>A |
| AA Mutation | p.Arg1105Gln(p.R1105Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838490:112838490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2896A>G |
| AA Mutation | p.Ser966Gly(p.S966G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112839856:112839856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4262G>A |
| AA Mutation | p.Ser1421Asn(p.S1421N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112821899:112821899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1316C>T |
| AA Mutation | p.Pro439Leu(p.P439L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112827932:112827932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1552A>G |
| AA Mutation | p.Thr518Ala(p.T518A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112828914:112828914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587783034 |
| CDS Mutation | c.1685C>T |
| AA Mutation | p.Thr562Met(p.T562M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840956:112840956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773125634 |
| CDS Mutation | c.5362C>T |
| AA Mutation | p.Arg1788Cys(p.R1788C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840755:112840755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5161G>T |
| AA Mutation | p.Gly1721Cys(p.G1721C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840931:112840931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748063409 |
| CDS Mutation | c.5337A>G |
| AA Mutation | p.Ile1779Met(p.I1779M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838360:112838360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2766T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838663:112838663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3069A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838696:112838696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840871:112840871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5277A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112828891:112828891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1662A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840661:112840661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112842344:112842344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555799753 |
| CDS Mutation | c.6750C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838417:112838417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2823A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112767238:112767238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.270A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838681:112838681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3087T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112835091:112835091(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1886delT |
| AA Mutation | p.Leu629Ter(p.L629*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112780890:112780890(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.636delA |
| AA Mutation | p.Lys212AsnfsTer7(p.K212Nfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840545:112840546(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4953_4954delTT |
| AA Mutation | p.Ser1652HisfsTer7(p.S1652Hfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112838774:112838774(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3183delA |
| AA Mutation | p.Lys1061AsnfsTer65(p.K1061Nfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112839947:112839986(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4356_4395delACCTAAAAATAAAGCACCTACTGCTGAAAAGAGAGAGAGT |
| AA Mutation | p.Pro1453AspfsTer7(p.P1453Dfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112842167:112842167(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775076289 |
| CDS Mutation | c.6579delA |
| AA Mutation | p.Val2194PhefsTer5(p.V2194Ffs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112841531:112841531(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5937delC |
| AA Mutation | p.Asn1979LysfsTer65(p.N1979Kfs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112828869:112828869(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1643delT |
| AA Mutation | p.Leu548Ter(p.L548*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112843272:112843272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7678C>T |
| AA Mutation | p.Arg2560Ter(p.R2560*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112838900:112838900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3306C>G |
| AA Mutation | p.Tyr1102Ter(p.Y1102*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112815564:112815564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137854568 |
| CDS Mutation | c.904C>T |
| AA Mutation | p.Arg302Ter(p.R302*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112839219:112839219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3625G>T |
| AA Mutation | p.Glu1209Ter(p.E1209*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112839942:112839942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913332 |
| CDS Mutation | c.4348C>T |
| AA Mutation | p.Arg1450Ter(p.R1450*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112842204:112842204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6610C>T |
| AA Mutation | p.Arg2204Ter(p.R2204*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112840320:112840320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4726G>T |
| AA Mutation | p.Glu1576Ter(p.E1576*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112838905:112838905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3311C>A |
| AA Mutation | p.Ser1104Ter(p.S1104*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112838985:112838985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3391C>T |
| AA Mutation | p.Gln1131Ter(p.Q1131*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112827194:112827194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137854580 |
| CDS Mutation | c.1495C>T |
| AA Mutation | p.Arg499Ter(p.R499*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000257430 |
| Start | 112840175:112840176(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4581_4582insTGTGTCTTTATAGCAGCATGATTTATACTCATTT |
| AA Mutation | p.Val1528CysfsTer7(p.V1528Cfs*7) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112843329:112843329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7735G>T |
| AA Mutation | p.Glu2579Ter(p.E2579*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257430 |
| Start | 112838934:112838934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913331 |
| CDS Mutation | c.3340C>T |
| AA Mutation | p.Arg1114Ter(p.R1114*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |