Mutation

Primary Site >> Stomach Cancer

Gene >> BCL9L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118901167:118901167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531414289
CDS Mutation	c.2576T>C
AA Mutation	p.Met859Thr(p.M859T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118901342:118901342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2401C>T
AA Mutation	p.Arg801Trp(p.R801W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118899053:118899053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566574462
CDS Mutation	c.3862C>T
AA Mutation	p.Arg1288Cys(p.R1288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118900050:118900050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3273G>A
AA Mutation	p.Met1091Ile(p.M1091I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118901279:118901279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2464G>A
AA Mutation	p.Ala822Thr(p.A822T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118900628:118900628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3115A>C
AA Mutation	p.Met1039Leu(p.M1039L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118902662:118902662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555442453
CDS Mutation	c.1081G>A
AA Mutation	p.Ala361Thr(p.A361T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118908308:118908308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557438958
CDS Mutation	c.374G>A
AA Mutation	p.Arg125Gln(p.R125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118900963:118900963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377431418
CDS Mutation	c.2780C>T
AA Mutation	p.Pro927Leu(p.P927L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118902265:118902265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781404269
CDS Mutation	c.1478C>T
AA Mutation	p.Pro493Leu(p.P493L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118899269:118899269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3646T>C
AA Mutation	p.Cys1216Arg(p.C1216R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118902590:118902590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372773894
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118899488:118899488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3427A>G
AA Mutation	p.Ser1143Gly(p.S1143G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334801
Start	118900196:118900196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3127A>G
AA Mutation	p.Thr1043Ala(p.T1043A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118900999:118900999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746679037
CDS Mutation	c.2744C>T
AA Mutation	p.Ser915Leu(p.S915L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000334801
Start	118902571:118902571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761142257
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391His(p.R391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118902690:118902690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118898520:118898520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763712696
CDS Mutation	c.4395G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118898703:118898703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140274068
CDS Mutation	c.4212C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118901121:118901121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2622G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118902714:118902714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334801
Start	118902135:118902135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118899403:118899403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3512delC
AA Mutation	p.Pro1171ArgfsTer32(p.P1171Rfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118899943:118899943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs751794665
CDS Mutation	c.3380delC
AA Mutation	p.Pro1127HisfsTer21(p.P1127Hfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118901800:118901800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1943delG
AA Mutation	p.Gly648AspfsTer23(p.G648Dfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118908587:118908587(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.95delC
AA Mutation	p.Pro32LeufsTer13(p.P32Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118902418:118902418(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1325delG
AA Mutation	p.Gly442AlafsTer21(p.G442Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118902295:118902295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1448delC
AA Mutation	p.Pro483ArgfsTer19(p.P483Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118902397:118902397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754310793
CDS Mutation	c.1346delC
AA Mutation	p.Pro449LeufsTer14(p.P449Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118898851:118898851(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4064delC
AA Mutation	p.Pro1355LeufsTer6(p.P1355Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118898865:118898865(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4050delC
AA Mutation	p.Lys1351ArgfsTer10(p.K1351Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118902265:118902265(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1478delC
AA Mutation	p.Pro493ArgfsTer9(p.P493Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000334801
Start	118902488:118902488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>T
AA Mutation	p.Arg419Ter(p.R419*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334801
Start	118902264:118902265(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1478dupC
AA Mutation	p.Gly495TrpfsTer22(p.G495Wfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript