Colon Cancer: Gene >> GPR119

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276218
Start	130384952:130384952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775958455
CDS Mutation	c.496G>A
AA Mutation	p.Val166Met(p.V166M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276218
Start	130384663:130384663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750313300
CDS Mutation	c.785G>A
AA Mutation	p.Arg262Gln(p.R262Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276218
Start	130384945:130384945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Ile(p.T168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276218
Start	130384473:130384473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276218
Start	130384989:130384989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR119

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276218
Start	130385327:130385327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121C>A
AA Mutation	p.Leu41Ile(p.L41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript