Primary Site >> Stomach Cancer
Gene >> COL4A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110462343:110462343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755820436 |
| CDS Mutation | c.1735C>T |
| AA Mutation | p.Arg579Cys(p.R579C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110457425:110457425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1422G>T |
| AA Mutation | p.Lys474Asn(p.K474N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110465516:110465516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888G>T |
| AA Mutation | p.Gly630Cys(p.G630C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110503934:110503934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4226G>T |
| AA Mutation | p.Arg1409Met(p.R1409M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110465507:110465507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771559117 |
| CDS Mutation | c.1879G>A |
| AA Mutation | p.Gly627Ser(p.G627S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110424813:110424813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.260A>G |
| AA Mutation | p.Lys87Arg(p.K87R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110458803:110458803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777186602 |
| CDS Mutation | c.1465G>A |
| AA Mutation | p.Asp489Asn(p.D489N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110480258:110480258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779357792 |
| CDS Mutation | c.2626G>A |
| AA Mutation | p.Ala876Thr(p.A876T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110503237:110503237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762275000 |
| CDS Mutation | c.3994G>A |
| AA Mutation | p.Gly1332Arg(p.G1332R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110478159:110478159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2582G>T |
| AA Mutation | p.Arg861Leu(p.R861L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110482578:110482578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2821G>A |
| AA Mutation | p.Gly941Arg(p.G941R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110512004:110512004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4952G>T |
| AA Mutation | p.Arg1651Leu(p.R1651L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110430557:110430557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.598C>T |
| AA Mutation | p.Arg200Cys(p.R200C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360467 |
| Start | 110478131:110478131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2554C>T |
| AA Mutation | p.Pro852Ser(p.P852S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360467 |
| Start | 110436295:110436295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763026854 |
| CDS Mutation | c.753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360467 |
| Start | 110424862:110424862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201777404 |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360467 |
| Start | 110504216:110504216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4354C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360467 |
| Start | 110467068:110467068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2067A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360467 |
| Start | 110308093:110308093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774171520 |
| CDS Mutation | c.69C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360467 |
| Start | 110503977:110503977(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4275delC |
| AA Mutation | p.Gly1426GlufsTer33(p.G1426Efs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360467 |
| Start | 110446860:110446860(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1077delA |
| AA Mutation | p.Gly360ValfsTer93(p.G360Vfs*93) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360467 |
| Start | 110462155:110462155(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1641delA |
| AA Mutation | p.Gly548GlufsTer23(p.G548Efs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360467 |
| Start | 110503976:110503977(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs34603892 |
| CDS Mutation | c.4275dupC |
| AA Mutation | p.Gly1426ArgfsTer30(p.G1426Rfs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |