Colon Cancer: Gene >> CEACAM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357396
Start	41810346:41810346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Ala207Thr(p.A207T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357396
Start	41797675:41797675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>T
AA Mutation	p.Val51Leu(p.V51L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357396
Start	41797803:41797803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782466052
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000357396
Start	41797725:41797725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>A
AA Mutation	p.Trp67Ter(p.W67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CEACAM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357396
Start	41797817:41797817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782329916
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357396
Start	41808848:41808848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377521292
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357396
Start	41808812:41808812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript