Primary Site >> Stomach Cancer
Gene >> KDM4A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43671771:43671771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1630G>A |
| AA Mutation | p.Val544Met(p.V544M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43697993:43697993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2821C>T |
| AA Mutation | p.Leu941Phe(p.L941F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43691565:43691565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2312T>C |
| AA Mutation | p.Leu771Pro(p.L771P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43690945:43690945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375427182 |
| CDS Mutation | c.2138C>T |
| AA Mutation | p.Ser713Leu(p.S713L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43683763:43683763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764794848 |
| CDS Mutation | c.1814G>A |
| AA Mutation | p.Arg605His(p.R605H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43691521:43691521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747618804 |
| CDS Mutation | c.2268G>T |
| AA Mutation | p.Lys756Asn(p.K756N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43671609:43671609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1468G>A |
| AA Mutation | p.Val490Met(p.V490M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43653282:43653282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.107C>T |
| AA Mutation | p.Ser36Phe(p.S36F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43694091:43694091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2473C>T |
| AA Mutation | p.Arg825Cys(p.R825C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43662918:43662918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140820309 |
| CDS Mutation | c.454C>T |
| AA Mutation | p.Arg152Trp(p.R152W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43671634:43671634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369667794 |
| CDS Mutation | c.1493G>A |
| AA Mutation | p.Arg498His(p.R498H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372396 |
| Start | 43655679:43655679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528781215 |
| CDS Mutation | c.227C>T |
| AA Mutation | p.Thr76Met(p.T76M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372396 |
| Start | 43665738:43665738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139088184 |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000372396 |
| Start | 43690894:43690894(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2092delC |
| AA Mutation | p.Gln698ArgfsTer8(p.Q698Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |