Mutation

Primary Site >> Stomach Cancer

Gene >> BCL9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147624202:147624202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3524G>A
AA Mutation	p.Gly1175Asp(p.G1175D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000234739
Start	147614616:147614616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560A>G
AA Mutation	p.Lys187Arg(p.K187R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147624078:147624078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782131021
CDS Mutation	c.3400C>T
AA Mutation	p.Arg1134Trp(p.R1134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147619963:147619963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782091140
CDS Mutation	c.1808G>A
AA Mutation	p.Arg603Gln(p.R603Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147619015:147619015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860C>A
AA Mutation	p.Pro287His(p.P287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147624366:147624366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587726690
CDS Mutation	c.3688G>A
AA Mutation	p.Gly1230Arg(p.G1230R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147623896:147623896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139858510
CDS Mutation	c.3218C>T
AA Mutation	p.Pro1073Leu(p.P1073L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147618824:147618824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>T
AA Mutation	p.Gln223His(p.Q223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147619792:147619792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782671101
CDS Mutation	c.1637C>T
AA Mutation	p.Pro546Leu(p.P546L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147623949:147623949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3271C>G
AA Mutation	p.Gln1091Glu(p.Q1091E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147624446:147624446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3768A>C
AA Mutation	p.Glu1256Asp(p.E1256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147622328:147622328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2960T>G
AA Mutation	p.Leu987Arg(p.L987R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147620155:147620155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782700818
CDS Mutation	c.2000G>A
AA Mutation	p.Arg667His(p.R667H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147619266:147619266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371893579
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Cys(p.R371C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147623848:147623848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3170G>A
AA Mutation	p.Gly1057Asp(p.G1057D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000234739
Start	147613145:147613145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782019322
CDS Mutation	c.316G>A
AA Mutation	p.Asp106Asn(p.D106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147613180:147613180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782538388
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147624365:147624365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201462277
CDS Mutation	c.3687C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147613021:147613021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147618869:147618869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.714C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147620135:147620135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147624251:147624251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3573A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234739
Start	147618890:147618890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147620875:147620875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2726delC
AA Mutation	p.Pro909LeufsTer57(p.P909Lfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147619695:147619695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781994033
CDS Mutation	c.1547delC
AA Mutation	p.Pro516LeufsTer5(p.P516Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147619176:147619176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1026delC
AA Mutation	p.Thr343HisfsTer53(p.T343Hfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147624866:147624866(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4193delC
AA Mutation	p.Pro1398HisfsTer3(p.P1398Hfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147615879:147615880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.638_639delCA
AA Mutation	p.Thr213ArgfsTer17(p.T213Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000234739
Start	147619290:147619290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135G>T
AA Mutation	p.Glu379Ter(p.E379*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234739
Start	147614519:147614520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.468dupC
AA Mutation	p.Ser157LeufsTer27(p.S157Lfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript