Colon Cancer: Gene >> OGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290291
Start	62812846:62812846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564432812
CDS Mutation	c.1231G>A
AA Mutation	p.Ala411Thr(p.A411T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290291
Start	62812346:62812346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777605843
CDS Mutation	c.731G>A
AA Mutation	p.Arg244Gln(p.R244Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290291
Start	62812595:62812595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>A
AA Mutation	p.Gly327Asp(p.G327D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290291
Start	62812414:62812414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Cys(p.R267C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290291
Start	62813049:62813049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290291
Start	62813553:62813553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772919866
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290291
Start	62813586:62813586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1975delG
AA Mutation	p.Glu659ArgfsTer55(p.E659Rfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OGFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290291
Start	62812579:62812579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373078338
CDS Mutation	c.964G>A
AA Mutation	p.Glu322Lys(p.E322K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript