Primary Site >> Stomach Cancer
Gene >> GRIN2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 10180360:10180360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.52T>C |
| AA Mutation | p.Trp18Arg(p.W18R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9938407:9938407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751692867 |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Val187Ile(p.V187I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9849853:9849853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231C>A |
| AA Mutation | p.Leu411Met(p.L411M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 10180161:10180161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.251C>T |
| AA Mutation | p.Thr84Met(p.T84M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9768913:9768913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2533C>G |
| AA Mutation | p.Leu845Val(p.L845V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9822312:9822312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2120A>C |
| AA Mutation | p.Lys707Thr(p.K707T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763823:9763823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3721C>T |
| AA Mutation | p.Arg1241Trp(p.R1241W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763607:9763607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3937C>T |
| AA Mutation | p.Leu1313Phe(p.L1313F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9768910:9768910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2536C>T |
| AA Mutation | p.Arg846Cys(p.R846C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763622:9763622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3922T>C |
| AA Mutation | p.Ser1308Pro(p.S1308P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9938021:9938021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945G>T |
| AA Mutation | p.Glu315Asp(p.E315D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764068:9764068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534440095 |
| CDS Mutation | c.3476G>A |
| AA Mutation | p.Arg1159His(p.R1159H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9849850:9849850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1234G>C |
| AA Mutation | p.Glu412Gln(p.E412Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 10180210:10180210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.202A>C |
| AA Mutation | p.Asn68His(p.N68H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9768897:9768897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2549C>T |
| AA Mutation | p.Thr850Met(p.T850M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763867:9763867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3677G>A |
| AA Mutation | p.Gly1226Asp(p.G1226D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9768995:9768995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2451G>T |
| AA Mutation | p.Met817Ile(p.M817I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9849829:9849829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1255G>A |
| AA Mutation | p.Val419Met(p.V419M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763418:9763418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4126C>T |
| AA Mutation | p.Arg1376Cys(p.R1376C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9849922:9849922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1162G>A |
| AA Mutation | p.Ala388Thr(p.A388T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9841042:9841042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391T>C |
| AA Mutation | p.Leu464Pro(p.L464P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9840728:9840728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1570T>G |
| AA Mutation | p.Phe524Val(p.F524V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764881:9764881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149698593 |
| CDS Mutation | c.2663C>T |
| AA Mutation | p.Thr888Met(p.T888M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763569:9763569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545080350 |
| CDS Mutation | c.3975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9829636:9829636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1794T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9829579:9829579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1851G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764493:9764493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773366584 |
| CDS Mutation | c.3051C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764661:9764661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs77705198 |
| CDS Mutation | c.2883C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764039:9764039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3505C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763836:9763836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780909404 |
| CDS Mutation | c.3708C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 10180277:10180277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9798401:9798401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2232C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9840669:9840669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758378272 |
| CDS Mutation | c.1629C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9764235:9764235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3309C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9763455:9763455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774385825 |
| CDS Mutation | c.4089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000330684 |
| Start | 9841008:9841008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774228933 |
| CDS Mutation | c.1425C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |