Colon Cancer: Gene >> TWIST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242261
Start	19116781:19116781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Glu181Lys(p.E181K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242261
Start	19116724:19116724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762445986
CDS Mutation	c.598G>A
AA Mutation	p.Ala200Thr(p.A200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242261
Start	19116970:19116970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Cys(p.R118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242261
Start	19116981:19116981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341A>G
AA Mutation	p.Asn114Ser(p.N114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242261
Start	19116938:19116938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748239205
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242261
Start	19116794:19116794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242261
Start	19116947:19116947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773150642
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TWIST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242261
Start	19116934:19116934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>A
AA Mutation	p.Ala130Thr(p.A130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242261
Start	19116935:19116935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript