Colon Cancer: Gene >> PROCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216968
Start	35174795:35174795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746777605
CDS Mutation	c.164C>T
AA Mutation	p.Thr55Met(p.T55M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216968
Start	35176275:35176275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>T
AA Mutation	p.Arg144Trp(p.R144W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216968
Start	35176739:35176739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145801152
CDS Mutation	c.643G>A
AA Mutation	p.Val215Ile(p.V215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216968
Start	35176430:35176430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216968
Start	35174781:35174781(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.155delG
AA Mutation	p.Gly52AspfsTer3(p.G52Dfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000216968
Start	35176407:35176407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>T
AA Mutation	p.Gln188Ter(p.Q188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PROCR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216968
Start	35176272:35176272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427T>G
AA Mutation	p.Phe143Val(p.F143V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript