Colon Cancer: Gene >> CHI3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203183723:203183723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147131854
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203179804:203179804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968A>T
AA Mutation	p.Asn323Ile(p.N323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203179859:203179859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768428982
CDS Mutation	c.913G>A
AA Mutation	p.Gly305Arg(p.G305R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203184608:203184608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>C
AA Mutation	p.Leu94Phe(p.L94F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203179558:203179558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>A
AA Mutation	p.Ala347Thr(p.A347T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255409
Start	203179553:203179553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146151706
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000255409
Start	203182852:203182852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>T
AA Mutation	p.Glu156Ter(p.E156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CHI3L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255409
Start	203182739:203182739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579G>T
AA Mutation	p.Lys193Asn(p.K193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript