Colon Cancer: Gene >> RABEP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28914517:28914517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754503497
CDS Mutation	c.613C>T
AA Mutation	p.Pro205Ser(p.P205S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28919847:28919847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758567963
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28911142:28911142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28906120:28906120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441His(p.R441H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28924547:28924547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Trp(p.R44W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358201
Start	28906158:28906158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777877547
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358201
Start	28914513:28914513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.617delC
AA Mutation	p.Pro206ArgfsTer8(p.P206Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RABEP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358201
Start	28919801:28919801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>T
AA Mutation	p.Glu139Asp(p.E139D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript