Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GLUL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182385791:182385791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572C>T
AA Mutation	p.Ala191Val(p.A191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182384632:182384632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182386294:182386294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437C>A
AA Mutation	p.Pro146His(p.P146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311223
Start	182388639:182388639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772977794
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311223
Start	182384597:182384597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369280031
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311223
Start	182387273:182387273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141126924
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311223
Start	182384567:182384567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759079464
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000311223
Start	182386255:182386255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GLUL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182384431:182384431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>A
AA Mutation	p.Asp366Asn(p.D366N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182384572:182384572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Cys(p.R319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311223
Start	182384449:182384449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078C>A
AA Mutation	p.Leu360Ile(p.L360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311223
Start	182387273:182387273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141126924
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript