Colon Cancer: Gene >> CCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000533244
Start	66605492:66605492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571T>C
AA Mutation	p.Trp191Arg(p.W191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000533244
Start	66605809:66605809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779C>T
AA Mutation	p.Ala260Val(p.A260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000533244
Start	66599615:66599615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407A>G
AA Mutation	p.Asp136Gly(p.D136G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000533244
Start	66605768:66605768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201606373
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000533244
Start	66599487:66599487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.285delG
AA Mutation	p.Pro96LeufsTer13(p.P96Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000533244
Start	66599486:66599487(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759691599
CDS Mutation	c.285dupG
AA Mutation	p.Pro96AlafsTer16(p.P96Afs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000533244
Start	66599254:66599254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746825506
CDS Mutation	c.250+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CCS

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000533244
Start	66605377:66605377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372097218
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript