Colon Cancer: Gene >> F11R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368026
Start	161001124:161001124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137T>C
AA Mutation	p.Val46Ala(p.V46A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368026
Start	161001082:161001082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373771702
CDS Mutation	c.179T>C
AA Mutation	p.Val60Ala(p.V60A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368026
Start	160999400:160999400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811A>C
AA Mutation	p.Lys271Gln(p.K271Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368026
Start	160999908:160999908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>A
AA Mutation	p.Pro221His(p.P221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368026
Start	161001310:161001310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> F11R

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368026
Start	161001024:161001024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237C>A
Mutation Classification	Silent
Feature Type	Transcript