Colon Cancer: Gene >> PCCB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251654
Start	136250541:136250541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Asp56Asn(p.D56N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251654
Start	136283935:136283935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148056730
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251654
Start	136261975:136261975(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.457delG
AA Mutation	p.Ala153LeufsTer3(p.A153Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PCCB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251654
Start	136326902:136326902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190T>G
AA Mutation	p.Phe397Cys(p.F397C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251654
Start	136255917:136255917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>A
AA Mutation	p.Ser82Asn(p.S82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251654
Start	136250489:136250489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>A
Mutation Classification	Silent
Feature Type	Transcript