Colon Cancer: Gene >> AGER

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375076
Start	32183569:32183569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17846806
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375076
Start	32183617:32183617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777428643
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375076
Start	32181397:32181397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072A>G
AA Mutation	p.Ile358Val(p.I358V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375076
Start	32182992:32182992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375076
Start	32182365:32182365(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.846delC
AA Mutation	p.Ser283AlafsTer4(p.S283Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AGER

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375076
Start	32183358:32183358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>T
AA Mutation	p.Ser129Phe(p.S129F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript