Colon Cancer: Gene >> CLPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35795208:35795208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150755879
CDS Mutation	c.277G>A
AA Mutation	p.Val93Met(p.V93M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35797258:35797258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529464575
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35795789:35795789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114191664
CDS Mutation	c.149C>T
AA Mutation	p.Ala50Val(p.A50V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35795166:35795166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748533143
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35797258:35797258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529464575
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259938
Start	35795735:35795735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203T>C
AA Mutation	p.Val68Ala(p.V68A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000259938
Start	35795278:35795278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript