Colon Cancer: Gene >> TWSG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262120
Start	9396363:9396363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>A
AA Mutation	p.Leu103Ile(p.L103I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262120
Start	9396307:9396307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251A>T
AA Mutation	p.Asp84Val(p.D84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262120
Start	9396510:9396510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454A>G
AA Mutation	p.Ser152Gly(p.S152G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262120
Start	9396410:9396410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750635347
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TWSG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262120
Start	9396381:9396381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>C
AA Mutation	p.Glu109Gln(p.E109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262120
Start	9396449:9396449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393G>T
AA Mutation	p.Glu131Asp(p.E131D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript