Colon Cancer: Gene >> AGXT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307503
Start	240877556:240877556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61729604
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307503
Start	240877571:240877571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307503
Start	240868892:240868892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307503
Start	240873006:240873006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548869946
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307503
Start	240878084:240878084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307503
Start	240878108:240878108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748054201
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AGXT

No Mutation Annotation!