Colon Cancer: Gene >> BCL2L11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393256
Start	111150115:111150115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775080943
CDS Mutation	c.466G>A
AA Mutation	p.Gly156Arg(p.G156R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393256
Start	111164208:111164208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758817904
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Cys(p.R192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393256
Start	111164167:111164167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.His178Arg(p.H178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393256
Start	111124113:111124114(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.368_369insA
AA Mutation	p.Phe124LeufsTer15(p.F124Lfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCL2L11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393256
Start	111124017:111124017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778682749
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript