Colon Cancer: Gene >> FANCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229769
Start	35456096:35456096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763151358
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229769
Start	35455909:35455909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229769
Start	35456296:35456296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746542545
CDS Mutation	c.798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229769
Start	35457937:35457938(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749898067
CDS Mutation	c.929dupC
AA Mutation	p.Val311SerfsTer2(p.V311Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FANCE

No Mutation Annotation!