Colon Cancer: Gene >> BCL10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370580
Start	85270729:85270729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>A
AA Mutation	p.Leu79Met(p.L79M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370580
Start	85270764:85270764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200A>C
AA Mutation	p.Lys67Thr(p.K67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370580
Start	85270642:85270642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322A>C
AA Mutation	p.Asn108His(p.N108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370580
Start	85267840:85267840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139473915
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370580
Start	85267830:85267830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764922765
CDS Mutation	c.499delT
AA Mutation	p.Ser167LeufsTer6(p.S167Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BCL10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370580
Start	85267820:85267820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509C>A
AA Mutation	p.Ser170Tyr(p.S170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370580
Start	85270827:85270828(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs387906351
CDS Mutation	c.136dupA
AA Mutation	p.Ile46AsnfsTer4(p.I46Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript