Colon Cancer: Gene >> CTH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370938
Start	70424384:70424384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775272253
CDS Mutation	c.556G>A
AA Mutation	p.Val186Met(p.V186M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370938
Start	70433929:70433929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979A>C
AA Mutation	p.Ile327Leu(p.I327L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370938
Start	70416028:70416028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241G>A
AA Mutation	p.Ala81Thr(p.A81T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000370938
Start	70430396:70430396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370938
Start	70438759:70438759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124G>A
AA Mutation	p.Arg375Gln(p.R375Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370938
Start	70435158:70435158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771762248
CDS Mutation	c.1033G>A
AA Mutation	p.Glu345Lys(p.E345K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript