Primary Site >> Stomach Cancer
Gene >> CDKN2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21970968:21970968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755927351 |
| CDS Mutation | c.391C>T |
| AA Mutation | p.Arg131Cys(p.R131C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971133:21971133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774633329 |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Ala76Thr(p.A76T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971115:21971115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.244G>A |
| AA Mutation | p.Val82Met(p.V82M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974761:21974761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.67G>C |
| AA Mutation | p.Gly23Arg(p.G23R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974781:21974781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.47T>G |
| AA Mutation | p.Leu16Arg(p.L16R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21970982:21970982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104894098 |
| CDS Mutation | c.377T>A |
| AA Mutation | p.Val126Asp(p.V126D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971139:21971139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760640852 |
| CDS Mutation | c.220G>T |
| AA Mutation | p.Asp74Tyr(p.D74Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971114:21971114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.245T>A |
| AA Mutation | p.Val82Glu(p.V82E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971112:21971112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913385 |
| CDS Mutation | c.247C>T |
| AA Mutation | p.His83Tyr(p.H83Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971120:21971120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.239G>A |
| AA Mutation | p.Arg80Gln(p.R80Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971134:21971134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971107:21971107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971191:21971191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.168C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971194:21971194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974717:21974717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971140:21971140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs730881679 |
| CDS Mutation | c.219C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304494 |
| Start | 21970957:21970957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974698:21974698(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.130delT |
| AA Mutation | p.Tyr44ThrfsTer9(p.Y44Tfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971025:21971025(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.334delC |
| AA Mutation | p.Arg112ValfsTer34(p.R112Vfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000304494 |
| Start | 21971121:21971121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913388 |
| CDS Mutation | c.238C>T |
| AA Mutation | p.Arg80Ter(p.R80*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000304494 |
| Start | 21971001:21971001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358G>T |
| AA Mutation | p.Glu120Ter(p.E120*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000304494 |
| Start | 21974696:21974696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.132C>A |
| AA Mutation | p.Tyr44Ter(p.Y44*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974680:21974680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.148C>T |
| AA Mutation | p.Gln50Ter(p.Q50*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304494 |
| Start | 21971089:21971090(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.269dupT |
| AA Mutation | p.Leu91ProfsTer29(p.L91Pfs*29) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304494 |
| Start | 21974721:21974722(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs398123152 |
| CDS Mutation | c.106dupG |
| AA Mutation | p.Ala36GlyfsTer8(p.A36Gfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |