Colon Cancer: Gene >> CA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85442112:85442112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85442111:85442111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773052803
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85442187:85442187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770535043
CDS Mutation	c.347C>T
AA Mutation	p.Ala116Val(p.A116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85444091:85444091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766830102
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Cys(p.R137C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85446230:85446230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142713454
CDS Mutation	c.596C>T
AA Mutation	p.Thr199Met(p.T199M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85442088:85442088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248C>A
AA Mutation	p.Pro83His(p.P83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285381
Start	85445173:85445173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200197384
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000285381
Start	85448103:85448103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779091963
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Ter(p.R245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285381
Start	85439877:85439877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200G>A
AA Mutation	p.Arg67Gln(p.R67Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript