Colon Cancer: Gene >> TAGLN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320307
Start	159919817:159919817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199A>C
AA Mutation	p.Asn67His(p.N67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320307
Start	159918856:159918856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369414441
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Cys(p.R182C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320307
Start	159918884:159918884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141740615
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320307
Start	159918836:159918836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147762227
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320307
Start	159920381:159920381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAGLN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320307
Start	159919779:159919779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>T
AA Mutation	p.Lys79Asn(p.K79N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript