Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CEACAM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41715219:41715219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150900406
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Cys(p.R225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41721068:41721068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918C>A
AA Mutation	p.Leu640Ile(p.L640I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41709943:41709943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328C>A
AA Mutation	p.Gln110Lys(p.Q110K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41715132:41715132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>C
AA Mutation	p.Gly196Arg(p.G196R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41720958:41720958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781903049
CDS Mutation	c.1808C>T
AA Mutation	p.Ser603Leu(p.S603L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221992
Start	41721088:41721088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144920263
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221992
Start	41709755:41709756(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.140_141insT
AA Mutation	p.Glu47AspfsTer25(p.E47Dfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CEACAM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41721098:41721098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1948A>G
AA Mutation	p.Asn650Asp(p.N650D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41720179:41720179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146319665
CDS Mutation	c.1742G>A
AA Mutation	p.Arg581His(p.R581H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221992
Start	41721068:41721068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918C>A
AA Mutation	p.Leu640Ile(p.L640I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript