Primary Site >> Stomach Cancer
Gene >> PRX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394654:40394654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767851512 |
| CDS Mutation | c.3698C>T |
| AA Mutation | p.Ala1233Val(p.A1233V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40396815:40396815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1537C>G |
| AA Mutation | p.Pro513Ala(p.P513A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40398655:40398655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770713710 |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Glu116Lys(p.E116K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40398700:40398700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.301C>T |
| AA Mutation | p.Pro101Ser(p.P101S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394507:40394507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753530396 |
| CDS Mutation | c.3845C>T |
| AA Mutation | p.Ser1282Leu(p.S1282L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40396163:40396163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2189C>A |
| AA Mutation | p.Pro730His(p.P730H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40395696:40395696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779463585 |
| CDS Mutation | c.2656G>A |
| AA Mutation | p.Glu886Lys(p.E886K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40395624:40395624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145203783 |
| CDS Mutation | c.2728G>A |
| AA Mutation | p.Ala910Thr(p.A910T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40395528:40395528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2824A>G |
| AA Mutation | p.Lys942Glu(p.K942E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394520:40394520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377639106 |
| CDS Mutation | c.3832G>A |
| AA Mutation | p.Asp1278Asn(p.D1278N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394046:40394046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4306C>T |
| AA Mutation | p.Arg1436Trp(p.R1436W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394643:40394643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3709G>A |
| AA Mutation | p.Ala1237Thr(p.A1237T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394087:40394087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142436702 |
| CDS Mutation | c.4265G>A |
| AA Mutation | p.Arg1422Gln(p.R1422Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394930:40394930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201233076 |
| CDS Mutation | c.3422C>T |
| AA Mutation | p.Ala1141Val(p.A1141V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394783:40394783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3569T>C |
| AA Mutation | p.Val1190Ala(p.V1190A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394044:40394044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4308G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324001 |
| Start | 40398641:40398641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324001 |
| Start | 40396726:40396726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1626G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324001 |
| Start | 40395316:40395316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767439555 |
| CDS Mutation | c.3036C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324001 |
| Start | 40397011:40397011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1341T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394176:40394176(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4176delG |
| AA Mutation | p.Gln1393ArgfsTer25(p.Q1393Rfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394155:40394155(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4197delC |
| AA Mutation | p.Lys1400SerfsTer18(p.K1400Sfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324001 |
| Start | 40394579:40394579(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3773delG |
| AA Mutation | p.Gly1258AlafsTer124(p.G1258Afs*124) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324001 |
| Start | 40397309:40397309(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1043delG |
| AA Mutation | p.Gly348GlufsTer8(p.G348Efs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324001 |
| Start | 40395099:40395099(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758500214 |
| CDS Mutation | c.3253delG |
| AA Mutation | p.Glu1085LysfsTer42(p.E1085Kfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324001 |
| Start | 40395663:40395663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756689732 |
| CDS Mutation | c.2689C>T |
| AA Mutation | p.Arg897Ter(p.R897*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |