Colon Cancer: Gene >> CTHRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330295
Start	103378231:103378231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141428810
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Cys(p.R193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000330295
Start	103375958:103375958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374084026
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330295
Start	103375835:103375835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767061518
CDS Mutation	c.248G>A
AA Mutation	p.Arg83Gln(p.R83Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330295
Start	103378232:103378232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs36115601
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000330295
Start	103382586:103382586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>T
AA Mutation	p.Glu240Ter(p.E240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CTHRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330295
Start	103378103:103378103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Lys(p.R150K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript