Colon Cancer: Gene >> GLIPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377960
Start	36150901:36150901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>A
AA Mutation	p.Glu86Lys(p.E86K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377960
Start	36162513:36162513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372441239
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377960
Start	36147850:36147850(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.83delC
AA Mutation	p.Pro28HisfsTer2(p.P28Hfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GLIPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377960
Start	36147846:36147846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74G>C
AA Mutation	p.Gly25Ala(p.G25A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377960
Start	36148570:36148570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201812895
CDS Mutation	c.146C>T
AA Mutation	p.Thr49Met(p.T49M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript