Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GLCCI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223145
Start	8003911:8003911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461A>G
AA Mutation	p.Asp154Gly(p.D154G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223145
Start	8022506:8022506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>T
AA Mutation	p.Glu211Asp(p.E211D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000223145
Start	8085017:8085017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1298C>T
AA Mutation	p.Ala433Val(p.A433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223145
Start	8071016:8071016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145013590
CDS Mutation	c.1062G>T
AA Mutation	p.Gln354His(p.Q354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223145
Start	8086220:8086220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223145
Start	8086511:8086511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GLCCI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223145
Start	8060160:8060160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769366305
CDS Mutation	c.878C>T
AA Mutation	p.Ser293Leu(p.S293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223145
Start	8003911:8003911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461A>G
AA Mutation	p.Asp154Gly(p.D154G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223145
Start	8085003:8085003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284C>A
Mutation Classification	Silent
Feature Type	Transcript