Colon Cancer: Gene >> CLEC4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8521229:8521229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606A>T
AA Mutation	p.Glu202Asp(p.E202D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8519027:8519027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251G>T
AA Mutation	p.Cys84Phe(p.C84F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8521222:8521222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>T
AA Mutation	p.Asn200Ile(p.N200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8519147:8519147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371C>G
AA Mutation	p.Thr124Arg(p.T124R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8520334:8520334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374210290
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8515245:8515245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8519042:8519042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266G>T
AA Mutation	p.Arg89Ile(p.R89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000299665
Start	8515328:8515329(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.121_121+1insAAATAATAATTCAAGAAGAGTTCTACTTT
AA Mutation	p.Val41GlufsTer11(p.V41Efs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8515295:8515295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
AA Mutation	p.Leu30Phe(p.L30F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299665
Start	8518212:8518212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199672302
CDS Mutation	c.170A>G
AA Mutation	p.Lys57Arg(p.K57R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript