Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250535
Start	115816366:115816366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32C>T
AA Mutation	p.Thr11Ile(p.T11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250535
Start	115816333:115816333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65T>C
AA Mutation	p.Leu22Pro(p.L22P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250535
Start	115816322:115816322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776077445
CDS Mutation	c.76G>A
AA Mutation	p.Asp26Asn(p.D26N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250535
Start	115811192:115811192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250535
Start	115806491:115806491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431A>G
AA Mutation	p.Asn144Ser(p.N144S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250535
Start	115805455:115805455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766064742
CDS Mutation	c.581C>T
AA Mutation	p.Ser194Leu(p.S194L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250535
Start	115811192:115811192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>A
Mutation Classification	Silent
Feature Type	Transcript