Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXJ2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8039907:8039907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>T
AA Mutation	p.Glu25Asp(p.E25D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8050614:8050614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1630C>T
AA Mutation	p.Arg544Cys(p.R544C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8044787:8044787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>T
AA Mutation	p.Val216Leu(p.V216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8044084:8044084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611A>G
AA Mutation	p.Tyr204Cys(p.Y204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162391
Start	8052829:8052829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775220607
CDS Mutation	c.1704C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000162391
Start	8048141:8048142(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1082dupC
AA Mutation	p.Val362CysfsTer52(p.V362Cfs*52)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FOXJ2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8048715:8048715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244G>A
AA Mutation	p.Cys415Tyr(p.C415Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000162391
Start	8049509:8049509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475C>T
AA Mutation	p.Pro492Leu(p.P492L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162391
Start	8052781:8052781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656G>A
Mutation Classification	Silent
Feature Type	Transcript