Primary Site >> Stomach Cancer
Gene >> LAMB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49121333:49121333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5290C>T |
| AA Mutation | p.Arg1764Trp(p.R1764W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49125020:49125020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764846938 |
| CDS Mutation | c.2870G>A |
| AA Mutation | p.Arg957Gln(p.R957Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49123319:49123319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149144377 |
| CDS Mutation | c.4037G>A |
| AA Mutation | p.Arg1346His(p.R1346H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49128753:49128753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775598935 |
| CDS Mutation | c.1798G>A |
| AA Mutation | p.Val600Met(p.V600M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49130826:49130826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144771072 |
| CDS Mutation | c.950G>A |
| AA Mutation | p.Arg317His(p.R317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49128675:49128675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753645487 |
| CDS Mutation | c.1876C>T |
| AA Mutation | p.Arg626Cys(p.R626C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49130234:49130234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759728774 |
| CDS Mutation | c.1222C>T |
| AA Mutation | p.Arg408Cys(p.R408C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122173:49122173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779316233 |
| CDS Mutation | c.4771C>T |
| AA Mutation | p.Arg1591Trp(p.R1591W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124784:49124784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776023210 |
| CDS Mutation | c.3026G>A |
| AA Mutation | p.Arg1009His(p.R1009H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131716:49131716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Arg156His(p.R156H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122337:49122337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747861189 |
| CDS Mutation | c.4607T>C |
| AA Mutation | p.Val1536Ala(p.V1536A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49123783:49123783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372230106 |
| CDS Mutation | c.3742C>T |
| AA Mutation | p.Arg1248Cys(p.R1248C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49129285:49129285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs36050330 |
| CDS Mutation | c.1558C>T |
| AA Mutation | p.Arg520Cys(p.R520C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49128576:49128576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1900C>A |
| AA Mutation | p.Gln634Lys(p.Q634K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124264:49124264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139821983 |
| CDS Mutation | c.3350G>A |
| AA Mutation | p.Arg1117His(p.R1117H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49126107:49126107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2204C>T |
| AA Mutation | p.Ala735Val(p.A735V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122027:49122027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4840G>A |
| AA Mutation | p.Ala1614Thr(p.A1614T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131432:49131432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770390029 |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Arg220His(p.R220H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124814:49124814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2996C>T |
| AA Mutation | p.Ala999Val(p.A999V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122221:49122221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754337557 |
| CDS Mutation | c.4723C>T |
| AA Mutation | p.Arg1575Cys(p.R1575C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49129069:49129069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1682G>A |
| AA Mutation | p.Arg561Gln(p.R561Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122801:49122801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4476G>T |
| AA Mutation | p.Gln1492His(p.Q1492H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131000:49131000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569945951 |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Ala289Thr(p.A289T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49121990:49121990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752674803 |
| CDS Mutation | c.4877G>A |
| AA Mutation | p.Arg1626Gln(p.R1626Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124484:49124484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3238G>A |
| AA Mutation | p.Ala1080Thr(p.A1080T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131081:49131081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.784C>A |
| AA Mutation | p.Pro262Thr(p.P262T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124834:49124834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2976T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49124581:49124581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373002075 |
| CDS Mutation | c.3141G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49123862:49123862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3663G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122201:49122201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4743T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49123766:49123766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3759C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122888:49122888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4389G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49130983:49130983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750121965 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49129987:49129987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146643686 |
| CDS Mutation | c.1257C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |