Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CEACAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000161559
Start	42522106:42522106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521C>T
AA Mutation	p.Thr174Ile(p.T174I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161559
Start	42511601:42511601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161559
Start	42527093:42527093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161559
Start	42509202:42509202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1488G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CEACAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000161559
Start	42519114:42519114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080C>A
AA Mutation	p.Phe360Leu(p.F360L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000161559
Start	42522138:42522138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>C
Mutation Classification	Silent
Feature Type	Transcript