Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXJ3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361346
Start	42227885:42227885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Trp(p.R176W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42191468:42191468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779227723
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Cys(p.R396C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42191494:42191494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377432876
CDS Mutation	c.1160C>T
AA Mutation	p.Pro387Leu(p.P387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42227948:42227948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>T
AA Mutation	p.Asp155Tyr(p.D155Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361346
Start	42181984:42181984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361346
Start	42181981:42181981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1689G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000361346
Start	42189306:42189306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450C>T
AA Mutation	p.Gln484Ter(p.Q484*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXJ3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42227963:42227963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448T>C
AA Mutation	p.Ser150Pro(p.S150P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42191426:42191426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228C>T
AA Mutation	p.Leu410Phe(p.L410F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361346
Start	42278407:42278407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310A>T
AA Mutation	p.Ile104Phe(p.I104F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript