Colon Cancer: Gene >> TCL1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402399
Start	95711775:95711775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>C
AA Mutation	p.Glu109Gln(p.E109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402399
Start	95713970:95713970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402399
Start	95712360:95712360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402399
Start	95713995:95713995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779175388
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_lost
Transcription ID	ENST00000402399
Start	95711755:95711755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345A>G
AA Mutation	p.Ter115TrpextTer15(p.*115Wext*15)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TCL1A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402399
Start	95712259:95712259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>A
Mutation Classification	Silent
Feature Type	Transcript