Colon Cancer: Gene >> SCD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370355
Start	100354548:100354548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>A
AA Mutation	p.Arg188His(p.R188H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370355
Start	100360838:100360838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200630764
CDS Mutation	c.985G>A
AA Mutation	p.Ala329Thr(p.A329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370355
Start	100360807:100360807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.954C>G
AA Mutation	p.Asn318Lys(p.N318K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370355
Start	100356603:100356603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719A>G
AA Mutation	p.Glu240Gly(p.E240G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370355
Start	100348102:100348102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000370355
Start	100354505:100354505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200497654
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Ter(p.R174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SCD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370355
Start	100354542:100354542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557T>C
AA Mutation	p.Leu186Pro(p.L186P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript