Primary Site >> Stomach Cancer
Gene >> PCDHGA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365783:141365783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1453G>A |
| AA Mutation | p.Ala485Thr(p.A485T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366006:141366006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760966863 |
| CDS Mutation | c.1676C>T |
| AA Mutation | p.Thr559Met(p.T559M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366618:141366618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781279706 |
| CDS Mutation | c.2288C>T |
| AA Mutation | p.Ser763Leu(p.S763L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366467:141366467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2137G>A |
| AA Mutation | p.Val713Met(p.V713M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366399:141366399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2069C>T |
| AA Mutation | p.Thr690Ile(p.T690I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365051:141365051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.721C>A |
| AA Mutation | p.Leu241Met(p.L241M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364833:141364833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503G>A |
| AA Mutation | p.Arg168Gln(p.R168Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364772:141364772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.442G>A |
| AA Mutation | p.Ala148Thr(p.A148T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366087:141366087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1757A>G |
| AA Mutation | p.Tyr586Cys(p.Y586C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366723:141366723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2393A>C |
| AA Mutation | p.Asp798Ala(p.D798A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366488:141366488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2158C>T |
| AA Mutation | p.His720Tyr(p.H720Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365228:141365228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898G>A |
| AA Mutation | p.Glu300Lys(p.E300K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366566:141366566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181587578 |
| CDS Mutation | c.2236G>A |
| AA Mutation | p.Val746Ile(p.V746I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364800:141364800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Ala157Val(p.A157V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365778:141365778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375101471 |
| CDS Mutation | c.1448A>G |
| AA Mutation | p.Asp483Gly(p.D483G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366219:141366219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1889G>A |
| AA Mutation | p.Arg630Gln(p.R630Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364982:141364982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745559474 |
| CDS Mutation | c.652G>A |
| AA Mutation | p.Gly218Arg(p.G218R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365344:141365344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1014G>T |
| AA Mutation | p.Gln338His(p.Q338H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365607:141365607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1277A>G |
| AA Mutation | p.Asp426Gly(p.D426G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366174:141366174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1844G>T |
| AA Mutation | p.Gly615Val(p.G615V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364523:141364523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193C>T |
| AA Mutation | p.Arg65Cys(p.R65C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366257:141366257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1927G>A |
| AA Mutation | p.Val643Met(p.V643M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365007:141365007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776739278 |
| CDS Mutation | c.677C>T |
| AA Mutation | p.Thr226Met(p.T226M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366052:141366052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1722C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364396:141364396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.66G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365998:141365998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374639173 |
| CDS Mutation | c.1668C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366313:141366313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1983C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365005:141365005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366538:141366538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2208C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366199:141366199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1869G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365137:141365137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141365152:141365152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747695499 |
| CDS Mutation | c.822C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141366694:141366694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2364C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000518069 |
| Start | 141364723:141364723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746438679 |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |