Primary Site >> Stomach Cancer
Gene >> ITGB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75736066:75736066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1673C>A |
| AA Mutation | p.Ser558Tyr(p.S558Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75750811:75750811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3606G>T |
| AA Mutation | p.Gln1202His(p.Q1202H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75730269:75730269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.767C>G |
| AA Mutation | p.Thr256Ser(p.T256S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727435:75727435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200966154 |
| CDS Mutation | c.194C>T |
| AA Mutation | p.Ala65Val(p.A65V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75752245:75752245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200409597 |
| CDS Mutation | c.3865C>T |
| AA Mutation | p.Arg1289Trp(p.R1289W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727461:75727461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772790459 |
| CDS Mutation | c.220C>T |
| AA Mutation | p.Arg74Trp(p.R74W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75757514:75757514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757045931 |
| CDS Mutation | c.5428A>G |
| AA Mutation | p.Thr1810Ala(p.T1810A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75754663:75754663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4406A>T |
| AA Mutation | p.Tyr1469Phe(p.Y1469F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75733669:75733669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1634G>A |
| AA Mutation | p.Arg545His(p.R545H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727260:75727260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146966502 |
| CDS Mutation | c.145G>A |
| AA Mutation | p.Ala49Thr(p.A49T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75757227:75757227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5246C>G |
| AA Mutation | p.Ala1749Gly(p.A1749G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75754594:75754594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755867749 |
| CDS Mutation | c.4337G>A |
| AA Mutation | p.Arg1446Gln(p.R1446Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727441:75727441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.200T>C |
| AA Mutation | p.Leu67Pro(p.L67P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75733615:75733615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1580G>A |
| AA Mutation | p.Gly527Asp(p.G527D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75739982:75739982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764528048 |
| CDS Mutation | c.2357G>A |
| AA Mutation | p.Gly786Asp(p.G786D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75731939:75731939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144804175 |
| CDS Mutation | c.1343C>T |
| AA Mutation | p.Ala448Val(p.A448V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75750803:75750803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75129664 |
| CDS Mutation | c.3598G>A |
| AA Mutation | p.Gly1200Arg(p.G1200R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75752282:75752282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3902G>A |
| AA Mutation | p.Arg1301His(p.R1301H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75754639:75754639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4382T>C |
| AA Mutation | p.Met1461Thr(p.M1461T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75752478:75752478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187296783 |
| CDS Mutation | c.4009G>A |
| AA Mutation | p.Ala1337Thr(p.A1337T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75751077:75751077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376494263 |
| CDS Mutation | c.3759C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75731859:75731859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372707561 |
| CDS Mutation | c.1263G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75752561:75752561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149807848 |
| CDS Mutation | c.4092C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75757073:75757073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752571680 |
| CDS Mutation | c.5184C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75736302:75736302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1776A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75740819:75740819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148787870 |
| CDS Mutation | c.2577C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75732213:75732213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149030156 |
| CDS Mutation | c.1428C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75737632:75737632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2208T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727440:75727440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.199C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75733595:75733595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538635871 |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75731323:75731323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000200181 |
| Start | 75749026:75749026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3297C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000200181 |
| Start | 75742440:75742440(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2734delC |
| AA Mutation | p.His912ThrfsTer68(p.H912Tfs*68) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000200181 |
| Start | 75750158:75750158(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3368delC |
| AA Mutation | p.Pro1123LeufsTer37(p.P1123Lfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000200181 |
| Start | 75729291:75729292(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs752657203 |
| CDS Mutation | c.600dupC |
| AA Mutation | p.Phe201LeufsTer15(p.F201Lfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000200181 |
| Start | 75751030:75751031(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3713dupT |
| AA Mutation | p.Ser1239GlufsTer4(p.S1239Efs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |