Primary Site >> Stomach Cancer
Gene >> LRRC4B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518223:50518223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763207062 |
| CDS Mutation | c.1490C>T |
| AA Mutation | p.Thr497Met(p.T497M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517777:50517777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1936G>A |
| AA Mutation | p.Gly646Arg(p.G646R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519346:50519346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.367C>T |
| AA Mutation | p.Arg123Cys(p.R123C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517875:50517875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1838G>A |
| AA Mutation | p.Arg613His(p.R613H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519160:50519160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.553C>T |
| AA Mutation | p.Arg185Trp(p.R185W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50548565:50548565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274A>G |
| AA Mutation | p.Asn92Asp(p.N92D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518820:50518820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893C>T |
| AA Mutation | p.Thr298Met(p.T298M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518698:50518698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1015C>T |
| AA Mutation | p.Arg339Cys(p.R339C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518980:50518980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774640697 |
| CDS Mutation | c.733C>T |
| AA Mutation | p.Arg245Cys(p.R245C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518305:50518305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1408G>A |
| AA Mutation | p.Gly470Ser(p.G470S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518370:50518370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761399852 |
| CDS Mutation | c.1343C>T |
| AA Mutation | p.Ser448Leu(p.S448L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518437:50518437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Val426Ile(p.V426I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518215:50518215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748276107 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Gly500Arg(p.G500R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518620:50518620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1093G>A |
| AA Mutation | p.Val365Ile(p.V365I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518512:50518512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1201G>A |
| AA Mutation | p.Gly401Ser(p.G401S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517834:50517834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746496641 |
| CDS Mutation | c.1879G>A |
| AA Mutation | p.Ala627Thr(p.A627T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517836:50517836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1877C>T |
| AA Mutation | p.Ala626Val(p.A626V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517711:50517711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2002G>T |
| AA Mutation | p.Ala668Ser(p.A668S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519111:50519111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759714186 |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Ala201Val(p.A201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518694:50518694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1019G>C |
| AA Mutation | p.Cys340Ser(p.C340S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518710:50518710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003A>G |
| AA Mutation | p.Thr335Ala(p.T335A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518247:50518247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1466C>T |
| AA Mutation | p.Thr489Met(p.T489M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519330:50519330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Gly128Asp(p.G128D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519409:50519409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.304C>T |
| AA Mutation | p.Arg102Trp(p.R102W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518459:50518459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1254C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517886:50517886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1827C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518186:50518186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368964372 |
| CDS Mutation | c.1527G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50519088:50519088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50517628:50517628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2085C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518519:50518519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1194G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518318:50518318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1395C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389201 |
| Start | 50518057:50518057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536138658 |
| CDS Mutation | c.1656G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |