Primary Site >> Stomach Cancer
Gene >> CELF4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273127:37273127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150441111 |
| CDS Mutation | c.838G>A |
| AA Mutation | p.Ala280Thr(p.A280T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273147:37273147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764874262 |
| CDS Mutation | c.818C>T |
| AA Mutation | p.Ala273Val(p.A273V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274830:37274830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Ala211Val(p.A211V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37565488:37565488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154G>C |
| AA Mutation | p.Asp52His(p.D52H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37565613:37565613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.29A>G |
| AA Mutation | p.Asn10Ser(p.N10S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253908:37253908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1364C>T |
| AA Mutation | p.Ala455Val(p.A455V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274451:37274451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661G>T |
| AA Mutation | p.Ala221Ser(p.A221S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273037:37273037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769180157 |
| CDS Mutation | c.928G>A |
| AA Mutation | p.Ala310Thr(p.A310T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37565488:37565488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Asp52Asn(p.D52N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273030:37273030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.935T>C |
| AA Mutation | p.Met312Thr(p.M312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253818:37253818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1454C>T |
| AA Mutation | p.Pro485Leu(p.P485L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253881:37253881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391G>A |
| AA Mutation | p.Gly464Asp(p.G464D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274339:37274339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.773T>C |
| AA Mutation | p.Phe258Ser(p.F258S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37565365:37565365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277A>G |
| AA Mutation | p.Met93Val(p.M93V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253911:37253911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1361G>A |
| AA Mutation | p.Ser454Asn(p.S454N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37270806:37270806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777172664 |
| CDS Mutation | c.1061C>T |
| AA Mutation | p.Ala354Val(p.A354V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37565391:37565391(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 | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253821:37253821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1451G>A |
| AA Mutation | p.Arg484His(p.R484H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274348:37274348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764C>T |
| AA Mutation | p.Ala255Val(p.A255V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273086:37273086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140525001 |
| CDS Mutation | c.879C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37253925:37253925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1347C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274320:37274320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561213595 |
| CDS Mutation | c.792C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37273146:37273146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145932686 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37275128:37275128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37270793:37270793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765790379 |
| CDS Mutation | c.1074C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420428 |
| Start | 37274329:37274329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182333668 |
| CDS Mutation | c.783C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |