Colon Cancer: Gene >> CA5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318636
Start	15764712:15764712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277C>A
AA Mutation	p.Leu93Ile(p.L93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318636
Start	15776717:15776717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318636
Start	15764733:15764733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.298T>C
AA Mutation	p.Tyr100His(p.Y100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318636
Start	15774323:15774323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147600421
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CA5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318636
Start	15782497:15782497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769895567
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Trp(p.R263W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318636
Start	15782558:15782559(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.848_849insAT
AA Mutation	p.Leu284SerfsTer5(p.L284Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript