Colon Cancer: Gene >> BCL2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31666004:31666004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647C>T
AA Mutation	p.Thr216Met(p.T216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31721857:31721857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>C
AA Mutation	p.Gln121Pro(p.Q121P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31722014:31722014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205A>C
AA Mutation	p.Thr69Pro(p.T69P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31721765:31721765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766818591
CDS Mutation	c.454G>A
AA Mutation	p.Val152Met(p.V152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31721894:31721894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325A>G
AA Mutation	p.Thr109Ala(p.T109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307677
Start	31665988:31665988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543917106
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307677
Start	31721769:31721769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307677
Start	31666045:31666046(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.605_606insTGTGGTG
AA Mutation	p.Glu202AspfsTer39(p.E202Dfs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCL2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307677
Start	31666040:31666040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Gln(p.R204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript