Primary Site >> Stomach Cancer
Gene >> SLC23A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4883667:4883667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799G>A |
| AA Mutation | p.Gly267Arg(p.G267R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4873995:4873995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1043G>A |
| AA Mutation | p.Arg348His(p.R348H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4862876:4862876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Ala463Val(p.A463V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4874082:4874082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.956C>T |
| AA Mutation | p.Ala319Val(p.A319V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4885862:4885862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530G>A |
| AA Mutation | p.Arg177Gln(p.R177Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4862862:4862862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201605928 |
| CDS Mutation | c.1402G>A |
| AA Mutation | p.Ala468Thr(p.A468T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4899567:4899567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377561504 |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Thr157Met(p.T157M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4899687:4899687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751107544 |
| CDS Mutation | c.350C>T |
| AA Mutation | p.Thr117Met(p.T117M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338244 |
| Start | 4862067:4862067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1505G>A |
| AA Mutation | p.Gly502Asp(p.G502D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338244 |
| Start | 4932545:4932545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338244 |
| Start | 4862893:4862893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1371C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338244 |
| Start | 4873973:4873973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1065G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338244 |
| Start | 4869992:4869992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147469332 |
| CDS Mutation | c.1164C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4857089:4857089(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1836delA |
| AA Mutation | p.Lys612AsnfsTer64(p.K612Nfs*64) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4862808:4862808(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1456delG |
| AA Mutation | p.Val486CysfsTer12(p.V486Cfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4883676:4883676(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.790delG |
| AA Mutation | p.Glu264ArgfsTer12(p.E264Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4869923:4869923(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751050083 |
| CDS Mutation | c.1233delC |
| AA Mutation | p.Ile412SerfsTer4(p.I412Sfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4857088:4857089(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1836dupA |
| AA Mutation | p.Tyr613IlefsTer32(p.Y613Ifs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338244 |
| Start | 4867782:4867783(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1343dupT |
| AA Mutation | p.Leu448PhefsTer58(p.L448Ffs*58) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |