Colon Cancer: Gene >> CDR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347230:22347230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100G>A
AA Mutation	p.Cys367Tyr(p.C367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347443:22347443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887T>C
AA Mutation	p.Leu296Pro(p.L296P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347326:22347326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004C>T
AA Mutation	p.Ala335Val(p.A335V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347480:22347480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850A>G
AA Mutation	p.Lys284Glu(p.K284E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347590:22347590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200274411
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347345:22347345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Glu329Lys(p.E329K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22349408:22349408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377T>C
AA Mutation	p.Ile126Thr(p.I126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268383
Start	22347520:22347520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268383
Start	22347729:22347729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.601delA
AA Mutation	p.Thr201GlnfsTer2(p.T201Qfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000268383
Start	22347558:22347558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770035745
CDS Mutation	c.772C>T
AA Mutation	p.Arg258Ter(p.R258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000268383
Start	22347555:22347555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775C>T
AA Mutation	p.Gln259Ter(p.Q259*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22364908:22364908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186A>C
AA Mutation	p.Glu62Asp(p.E62D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268383
Start	22347590:22347590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200274411
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268383
Start	22347361:22347361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201108991
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript