Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RBFOX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000580155
Start	79096676:79096676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>A
AA Mutation	p.Gly258Arg(p.G258R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000580155
Start	79096664:79096664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Ala262Thr(p.A262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580155
Start	79097375:79097375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580155
Start	79097324:79097324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580155
Start	79094526:79094526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000580155
Start	79097309:79097309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.738delC
AA Mutation	p.Ile247SerfsTer77(p.I247Sfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RBFOX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000580155
Start	79106752:79106752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259C>T
AA Mutation	p.Leu87Phe(p.L87F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000580155
Start	79104084:79104084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Trp(p.R135W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580155
Start	79097723:79097723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript