Colon Cancer: Gene >> BCL2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267953
Start	79970752:79970752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368C>T
AA Mutation	p.Ala123Val(p.A123V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000267953
Start	79961173:79961173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422A>C
AA Mutation	p.Glu141Ala(p.E141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267953
Start	79970745:79970745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375C>A
AA Mutation	p.Phe125Leu(p.F125L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267953
Start	79970880:79970880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240A>C
AA Mutation	p.Glu80Asp(p.E80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267953
Start	79970709:79970709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147879852
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267953
Start	79970871:79970871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267953
Start	79961122:79961123(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.472_473insAAAGTTGTTTATTTAAAAG
AA Mutation	p.Leu158GlnfsTer15(p.L158Qfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000267953
Start	79970698:79970698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BCL2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267953
Start	79970762:79970762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358T>C
AA Mutation	p.Tyr120His(p.Y120H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript