Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GLCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69268502:69268502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112A>G
AA Mutation	p.Lys371Arg(p.K371R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69261276:69261276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202049062
CDS Mutation	c.776C>T
AA Mutation	p.Ala259Val(p.A259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69256348:69256348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561898890
CDS Mutation	c.542A>G
AA Mutation	p.Asn181Ser(p.N181S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69255858:69255858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138637994
CDS Mutation	c.52G>A
AA Mutation	p.Ala18Thr(p.A18T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69255825:69255825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749027018
CDS Mutation	c.19C>T
AA Mutation	p.Arg7Trp(p.R7W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69268925:69268925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535T>G
AA Mutation	p.Phe512Cys(p.F512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69256125:69256125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319A>T
AA Mutation	p.Ile107Phe(p.I107F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69256030:69256030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224A>G
AA Mutation	p.Glu75Gly(p.E75G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261858
Start	69268311:69268311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261858
Start	69268524:69268524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261858
Start	69268875:69268875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GLCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69268974:69268974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1584A>C
AA Mutation	p.Glu528Asp(p.E528D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69255928:69255928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756061835
CDS Mutation	c.122G>A
AA Mutation	p.Arg41Gln(p.R41Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69256326:69256326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520T>C
AA Mutation	p.Phe174Leu(p.F174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69255858:69255858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138637994
CDS Mutation	c.52G>A
AA Mutation	p.Ala18Thr(p.A18T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69256268:69256268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
AA Mutation	p.Phe154Leu(p.F154L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261858
Start	69268828:69268828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438C>A
AA Mutation	p.Leu480Ile(p.L480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261858
Start	69261241:69261241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261858
Start	69268980:69268980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530064318
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript