Colon Cancer: Gene >> CLEC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78030674:78030674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454G>A
AA Mutation	p.Asp152Asn(p.D152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78030797:78030797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761179747
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Cys(p.R193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78030584:78030584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147323906
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78028131:78028131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167A>G
AA Mutation	p.Gln56Arg(p.Q56R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78030617:78030617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>T
AA Mutation	p.Gly133Cys(p.G133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299642
Start	78030615:78030615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395C>T
AA Mutation	p.Pro132Leu(p.P132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript