Primary Site >> Stomach Cancer
Gene >> LMX1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165213717:165213717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758502343 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Pro198Leu(p.P198L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165353193:165353193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376967723 |
| CDS Mutation | c.146G>A |
| AA Mutation | p.Arg49Gln(p.R49Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165355514:165355514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.46G>A |
| AA Mutation | p.Asp16Asn(p.D16N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165249600:165249600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778377042 |
| CDS Mutation | c.304G>A |
| AA Mutation | p.Ala102Thr(p.A102T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165210731:165210731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764888037 |
| CDS Mutation | c.715G>A |
| AA Mutation | p.Val239Ile(p.V239I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165213714:165213714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596G>A |
| AA Mutation | p.Arg199Lys(p.R199K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165205914:165205914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768850154 |
| CDS Mutation | c.938G>A |
| AA Mutation | p.Arg313Gln(p.R313Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165353124:165353124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.215C>A |
| AA Mutation | p.Thr72Asn(p.T72N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165355520:165355520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.40G>A |
| AA Mutation | p.Ala14Thr(p.A14T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165205966:165205966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.886C>T |
| AA Mutation | p.Pro296Ser(p.P296S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294816 |
| Start | 165249590:165249590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314A>C |
| AA Mutation | p.Glu105Ala(p.E105A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294816 |
| Start | 165213737:165213737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.573C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294816 |
| Start | 165213755:165213755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.555T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294816 |
| Start | 165249415:165249415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294816 |
| Start | 165353162:165353162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527370820 |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |