Colon Cancer: Gene >> FSCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5603943:5603943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751111507
CDS Mutation	c.1192C>T
AA Mutation	p.Arg398Cys(p.R398C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5603899:5603899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755808795
CDS Mutation	c.1148G>A
AA Mutation	p.Arg383His(p.R383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5605377:5605377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385C>T
AA Mutation	p.Ala462Val(p.A462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5603898:5603898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Cys(p.R383C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5605325:5605325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756163037
CDS Mutation	c.1333G>A
AA Mutation	p.Gly445Ser(p.G445S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5593262:5593262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326G>A
AA Mutation	p.Arg109Gln(p.R109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382361
Start	5603529:5603529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382361
Start	5605390:5605390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568861608
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382361
Start	5593377:5593377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FSCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382361
Start	5603890:5603890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139T>C
AA Mutation	p.Leu380Pro(p.L380P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382361
Start	5603321:5603321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript