Colon Cancer: Gene >> FSTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120404878:120404878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>T
AA Mutation	p.Asp186Tyr(p.D186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120403254:120403254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
AA Mutation	p.Pro228Ser(p.P228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120403262:120403262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674C>A
AA Mutation	p.Ser225Tyr(p.S225Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120411901:120411901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Cys84Tyr(p.C84Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120409623:120409623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376856380
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120402897:120402897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143843913
CDS Mutation	c.716C>T
AA Mutation	p.Thr239Met(p.T239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295633
Start	120399904:120399904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000295633
Start	120411854:120411854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>T
AA Mutation	p.Glu100Ter(p.E100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000295633
Start	120399900:120399900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865G>T
AA Mutation	p.Glu289Ter(p.E289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FSTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120409626:120409626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554312023
CDS Mutation	c.368G>A
AA Mutation	p.Arg123His(p.R123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295633
Start	120409629:120409629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748013373
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295633
Start	120396958:120396958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295633
Start	120404885:120404885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138829728
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript