Primary Site >> Stomach Cancer
Gene >> CACNA2D4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1914910:1914910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555700156 |
| CDS Mutation | c.253G>A |
| AA Mutation | p.Gly85Ser(p.G85S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1856210:1856210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2028C>A |
| AA Mutation | p.His676Gln(p.H676Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1795757:1795757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3137C>T |
| AA Mutation | p.Pro1046Leu(p.P1046L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1854038:1854038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2159A>G |
| AA Mutation | p.Glu720Gly(p.E720G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1874662:1874662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1820T>C |
| AA Mutation | p.Met607Thr(p.M607T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1882902:1882902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376591807 |
| CDS Mutation | c.1450G>A |
| AA Mutation | p.Asp484Asn(p.D484N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1858591:1858591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770622451 |
| CDS Mutation | c.1994C>T |
| AA Mutation | p.Thr665Met(p.T665M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1886260:1886260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956A>T |
| AA Mutation | p.Asp319Val(p.D319V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1884273:1884273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748328734 |
| CDS Mutation | c.1321C>T |
| AA Mutation | p.Arg441Cys(p.R441C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1882929:1882929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755333586 |
| CDS Mutation | c.1423C>T |
| AA Mutation | p.Arg475Cys(p.R475C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1793687:1793687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3382G>A |
| AA Mutation | p.Ala1128Thr(p.A1128T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1882979:1882979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373696894 |
| CDS Mutation | c.1373C>T |
| AA Mutation | p.Thr458Met(p.T458M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1795352:1795352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3256C>T |
| AA Mutation | p.Arg1086Cys(p.R1086C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382722 |
| Start | 1907493:1907493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755897098 |
| CDS Mutation | c.728C>T |
| AA Mutation | p.Thr243Met(p.T243M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1909927:1909927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752053429 |
| CDS Mutation | c.465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1907972:1907972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1878330:1878330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186895987 |
| CDS Mutation | c.1704C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1795765:1795765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3129G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1882939:1882939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78872077 |
| CDS Mutation | c.1413C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382722 |
| Start | 1914908:1914908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375466678 |
| CDS Mutation | c.255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |