Primary Site >> Stomach Cancer
Gene >> ITIH5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7642006:7642006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.220C>A |
| AA Mutation | p.Leu74Met(p.L74M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566345:7566345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2212C>T |
| AA Mutation | p.Arg738Cys(p.R738C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7563340:7563340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2572G>T |
| AA Mutation | p.Gly858Trp(p.G858W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566204:7566204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2353G>A |
| AA Mutation | p.Gly785Arg(p.G785R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576971:7576971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112992012 |
| CDS Mutation | c.1460G>A |
| AA Mutation | p.Arg487His(p.R487H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7616071:7616071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850T>G |
| AA Mutation | p.Phe284Val(p.F284V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7642038:7642038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376012598 |
| CDS Mutation | c.188G>A |
| AA Mutation | p.Arg63His(p.R63H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637305:7637305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.575T>C |
| AA Mutation | p.Leu192Pro(p.L192P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566153:7566153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2404G>A |
| AA Mutation | p.Gly802Ser(p.G802S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637419:7637419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Ala154Val(p.A154V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566332:7566332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560482680 |
| CDS Mutation | c.2225G>A |
| AA Mutation | p.Arg742His(p.R742H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7585928:7585928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1081T>A |
| AA Mutation | p.Tyr361Asn(p.Y361N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7640771:7640771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.384A>C |
| AA Mutation | p.Lys128Asn(p.K128N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576906:7576906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567773535 |
| CDS Mutation | c.1525G>A |
| AA Mutation | p.Gly509Ser(p.G509S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637383:7637383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.497G>A |
| AA Mutation | p.Arg166His(p.R166H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7579987:7579987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185691581 |
| CDS Mutation | c.1186C>T |
| AA Mutation | p.Arg396Trp(p.R396W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7616010:7616010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911C>T |
| AA Mutation | p.Ala304Val(p.A304V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637296:7637296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584C>T |
| AA Mutation | p.Ala195Val(p.A195V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7579969:7579969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768826767 |
| CDS Mutation | c.1204G>A |
| AA Mutation | p.Val402Ile(p.V402I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7616034:7616034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.887T>C |
| AA Mutation | p.Val296Ala(p.V296A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576978:7576978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1453G>A |
| AA Mutation | p.Asp485Asn(p.D485N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7563378:7563378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2534T>C |
| AA Mutation | p.Phe845Ser(p.F845S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576608:7576608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1823T>C |
| AA Mutation | p.Leu608Pro(p.L608P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7616026:7616026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199952014 |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Val299Met(p.V299M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566383:7566383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2174T>C |
| AA Mutation | p.Ile725Thr(p.I725T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7641942:7641942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373965718 |
| CDS Mutation | c.284T>C |
| AA Mutation | p.Ile95Thr(p.I95T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576605:7576605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1826C>G |
| AA Mutation | p.Ala609Gly(p.A609G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576496:7576496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376071464 |
| CDS Mutation | c.1935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576652:7576652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181083224 |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7585947:7585947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147313445 |
| CDS Mutation | c.1062C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576742:7576742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1689A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7566043:7566043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2514C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576712:7576712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758245316 |
| CDS Mutation | c.1719C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7569708:7569708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2109C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7579766:7579766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373527198 |
| CDS Mutation | c.1407G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576955:7576955(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1476delC |
| AA Mutation | p.Ser493AlafsTer49(p.S493Afs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637413:7637413(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.467delT |
| AA Mutation | p.Phe156SerfsTer2(p.F156Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576954:7576955(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1476dupC |
| AA Mutation | p.Ser493GlnfsTer44(p.S493Qfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |