Colon Cancer: Gene >> CPB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46055782:46055782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067G>A
AA Mutation	p.Gly356Asp(p.G356D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46073973:46073973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Phe(p.S164F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46105005:46105005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5A>C
AA Mutation	p.Lys2Thr(p.K2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46055774:46055774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075T>G
AA Mutation	p.Ser359Ala(p.S359A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000181383
Start	46084326:46084326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374272287
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000181383
Start	46084233:46084233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201399827
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181383
Start	46082485:46082485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.340delC
AA Mutation	p.Arg114GlufsTer13(p.R114Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181383
Start	46084281:46084281(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.213delT
AA Mutation	p.Phe71LeufsTer2(p.F71Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181383
Start	46084296:46084296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.198delA
AA Mutation	p.Lys66AsnfsTer7(p.K66Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000181383
Start	46084280:46084281(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.213dupT
AA Mutation	p.Val72CysfsTer5(p.V72Cfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CPB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46105003:46105003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7C>T
AA Mutation	p.Leu3Phe(p.L3F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46058207:46058207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376421547
CDS Mutation	c.971G>A
AA Mutation	p.Arg324Gln(p.R324Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000181383
Start	46078852:46078852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Thr145Ile(p.T145I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript