Colon Cancer: Gene >> STC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290271
Start	23851513:23851513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>C
AA Mutation	p.Glu94Gln(p.E94Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290271
Start	23851348:23851348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139152218
CDS Mutation	c.445G>A
AA Mutation	p.Val149Ile(p.V149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290271
Start	23844911:23844911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603C>A
AA Mutation	p.His201Gln(p.H201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290271
Start	23851509:23851509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>A
AA Mutation	p.Ser95Asn(p.S95N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290271
Start	23854449:23854449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290271
Start	23852340:23852340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163G>A
AA Mutation	p.Gly55Arg(p.G55R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290271
Start	23851340:23851340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290271
Start	23851349:23851349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444C>A
Mutation Classification	Silent
Feature Type	Transcript