Colon Cancer: Gene >> CLEC7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304084
Start	10118568:10118568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634A>G
AA Mutation	p.Thr212Ala(p.T212A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304084
Start	10118577:10118577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625A>G
AA Mutation	p.Thr209Ala(p.T209A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304084
Start	10129998:10129998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304084
Start	10127753:10127753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196A>G
AA Mutation	p.Thr66Ala(p.T66A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304084
Start	10130078:10130078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5A>C
AA Mutation	p.Glu2Ala(p.E2A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000304084
Start	10123243:10123243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript