Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ERBB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085070:56085070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Val104Met(p.V104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088653:56088653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985A>G
AA Mutation	p.Lys329Glu(p.K329E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095757:56095757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772747085
CDS Mutation	c.2006G>A
AA Mutation	p.Arg669His(p.R669H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56099653:56099653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2845A>G
AA Mutation	p.Met949Val(p.M949V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56098857:56098857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2791G>A
AA Mutation	p.Ala931Thr(p.A931T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267101
Start	56094188:56094188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748595358
CDS Mutation	c.1703C>T
AA Mutation	p.Ser568Leu(p.S568L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085138:56085138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>G
AA Mutation	p.Asn126Lys(p.N126K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088098:56088098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810C>G
AA Mutation	p.Phe270Leu(p.F270L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088061:56088061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258His(p.R258H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093493:56093493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>T
AA Mutation	p.Arg475Trp(p.R475W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56095750:56095750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775164134
CDS Mutation	c.1999C>T
AA Mutation	p.Arg667Cys(p.R667C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085068:56085068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778104039
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56087843:56087843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662C>T
AA Mutation	p.Pro221Leu(p.P221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56099967:56099967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3067G>A
AA Mutation	p.Ala1023Thr(p.A1023T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101970:56101970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3944G>A
AA Mutation	p.Ser1315Asn(p.S1315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56088073:56088073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785C>A
AA Mutation	p.Pro262His(p.P262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267101
Start	56098759:56098759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2693G>A
AA Mutation	p.Gly898Asp(p.G898D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56098849:56098849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2783A>G
AA Mutation	p.Glu928Gly(p.E928G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56098896:56098896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2830A>C
AA Mutation	p.Met944Leu(p.M944L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101239:56101239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2271188
CDS Mutation	c.3380G>A
AA Mutation	p.Arg1127His(p.R1127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56085114:56085114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775223707
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56094428:56094428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267101
Start	56099987:56099987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267101
Start	56097178:56097178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2413delG
AA Mutation	p.Ala805HisfsTer95(p.A805Hfs*95)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267101
Start	56101093:56101093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3238delC
AA Mutation	p.Arg1080ValfsTer22(p.R1080Vfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267101
Start	56097177:56097178(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2413dupG
AA Mutation	p.Ala805GlyfsTer22(p.A805Gfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ERBB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56093845:56093845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779911233
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Gln(p.R521Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56101080:56101080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3221G>A
AA Mutation	p.Ser1074Asn(p.S1074N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56085070:56085070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Val104Met(p.V104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56083847:56083847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179T>G
AA Mutation	p.Met60Arg(p.M60R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267101
Start	56097070:56097070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2300A>G
AA Mutation	p.Asp767Gly(p.D767G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267101
Start	56101117:56101118(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3264_3274dupACGGGGATGCC
AA Mutation	p.Leu1092HisfsTer14(p.L1092Hfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript