Primary Site >> Stomach Cancer
Gene >> PLXNA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127020262:127020262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3956T>C |
| AA Mutation | p.Ile1319Thr(p.I1319T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127022121:127022121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766170133 |
| CDS Mutation | c.4075G>A |
| AA Mutation | p.Gly1359Arg(p.G1359R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989248:126989248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749036813 |
| CDS Mutation | c.655G>A |
| AA Mutation | p.Val219Met(p.V219M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030047:127030047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760086877 |
| CDS Mutation | c.5044C>T |
| AA Mutation | p.Arg1682Trp(p.R1682W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127016599:127016599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753534974 |
| CDS Mutation | c.3097G>A |
| AA Mutation | p.Ala1033Thr(p.A1033T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127022214:127022214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4168G>A |
| AA Mutation | p.Ala1390Thr(p.A1390T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014293:127014293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2522A>G |
| AA Mutation | p.His841Arg(p.H841R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127022792:127022792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4336A>G |
| AA Mutation | p.Thr1446Ala(p.T1446A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127011983:127011983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201387860 |
| CDS Mutation | c.2138C>T |
| AA Mutation | p.Thr713Met(p.T713M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127032476:127032476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761304812 |
| CDS Mutation | c.5321C>T |
| AA Mutation | p.Ser1774Leu(p.S1774L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127022230:127022230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775284582 |
| CDS Mutation | c.4184C>T |
| AA Mutation | p.Thr1395Met(p.T1395M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030300:127030300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5119C>T |
| AA Mutation | p.Arg1707Trp(p.R1707W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014512:127014512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770145599 |
| CDS Mutation | c.2639C>T |
| AA Mutation | p.Thr880Met(p.T880M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 126988752:126988752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.159C>G |
| AA Mutation | p.His53Gln(p.H53Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127004895:127004895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751844491 |
| CDS Mutation | c.1630C>T |
| AA Mutation | p.Arg544Trp(p.R544W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127004989:127004989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1724T>C |
| AA Mutation | p.Val575Ala(p.V575A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030407:127030407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5226C>A |
| AA Mutation | p.Ser1742Arg(p.S1742R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989531:126989531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.938A>G |
| AA Mutation | p.Gln313Arg(p.Q313R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127016605:127016605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3103C>A |
| AA Mutation | p.Leu1035Ile(p.L1035I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127022196:127022196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368240880 |
| CDS Mutation | c.4150C>T |
| AA Mutation | p.Arg1384Cys(p.R1384C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127032575:127032575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5420C>T |
| AA Mutation | p.Pro1807Leu(p.P1807L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989479:126989479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202007314 |
| CDS Mutation | c.886G>A |
| AA Mutation | p.Val296Ile(p.V296I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127028001:127028001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4424G>A |
| AA Mutation | p.Gly1475Asp(p.G1475D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014317:127014317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2546C>T |
| AA Mutation | p.Ala849Val(p.A849V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030280:127030280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5099C>A |
| AA Mutation | p.Thr1700Asn(p.T1700N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000393409 |
| Start | 127012157:127012157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757936424 |
| CDS Mutation | c.2312C>T |
| AA Mutation | p.Ser771Leu(p.S771L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127006163:127006163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1982G>A |
| AA Mutation | p.Cys661Tyr(p.C661Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014799:127014799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765821774 |
| CDS Mutation | c.2845C>T |
| AA Mutation | p.Arg949Cys(p.R949C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127029503:127029503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4837T>C |
| AA Mutation | p.Ser1613Pro(p.S1613P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127017876:127017876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3644G>A |
| AA Mutation | p.Gly1215Glu(p.G1215E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014623:127014623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763616398 |
| CDS Mutation | c.2750C>T |
| AA Mutation | p.Ala917Val(p.A917V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014802:127014802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758567414 |
| CDS Mutation | c.2848G>A |
| AA Mutation | p.Ala950Thr(p.A950T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030257:127030257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5076G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127005131:127005131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145552902 |
| CDS Mutation | c.1785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127016613:127016613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3111C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127005224:127005224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184131664 |
| CDS Mutation | c.1878G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127012047:127012047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144586368 |
| CDS Mutation | c.2202G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127017544:127017544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148780407 |
| CDS Mutation | c.3396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126988776:126988776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373400719 |
| CDS Mutation | c.183C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014741:127014741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2787C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127030317:127030317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377038275 |
| CDS Mutation | c.5136G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126988884:126988884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373197049 |
| CDS Mutation | c.291G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127005209:127005209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534632249 |
| CDS Mutation | c.1863C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127017490:127017490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014028:127014028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147176760 |
| CDS Mutation | c.2322C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989103:126989103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.510G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127005155:127005155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1809C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989178:126989178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779765951 |
| CDS Mutation | c.585C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127006131:127006131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1950G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127029457:127029457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750660306 |
| CDS Mutation | c.4791G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127017823:127017823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3591T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127032561:127032561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375428929 |
| CDS Mutation | c.5406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126991398:126991398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1209T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127006149:127006149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751981690 |
| CDS Mutation | c.1968C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127011993:127011993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2148C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 126989682:126989682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1089G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393409 |
| Start | 127014513:127014513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373034872 |
| CDS Mutation | c.2640G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |