Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOXI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388920
Start	127737766:127737766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000388920
Start	127738808:127738808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>T
AA Mutation	p.Ala267Val(p.A267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000388920
Start	127738547:127738547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539C>T
AA Mutation	p.Pro180Leu(p.P180L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000388920
Start	127738648:127738648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640G>T
AA Mutation	p.Gly214Trp(p.G214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388920
Start	127737546:127737546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388920
Start	127738911:127738911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745498954
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388920
Start	127738820:127738820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>A
AA Mutation	p.Ser271Tyr(p.S271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388920
Start	127738572:127738572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388920
Start	127738791:127738791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748678951
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript