Colon Cancer: Gene >> TACSTD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371225
Start	58576273:58576273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884T>C
AA Mutation	p.Leu295Pro(p.L295P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371225
Start	58576394:58576394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Cys(p.R255C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371225
Start	58576681:58576681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>A
AA Mutation	p.Arg159His(p.R159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371225
Start	58576587:58576587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000371225
Start	58576412:58576412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>T
AA Mutation	p.Glu249Ter(p.E249*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TACSTD2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371225
Start	58576335:58576335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript