Colon Cancer: Gene >> TMPRSS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000437212
Start	118104721:118104721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774877636
CDS Mutation	c.341A>G
AA Mutation	p.Gln114Arg(p.Q114R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000437212
Start	118113304:118113304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144368038
CDS Mutation	c.779C>T
AA Mutation	p.Ala260Val(p.A260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000437212
Start	118113268:118113268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TMPRSS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000437212
Start	118113300:118113300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61663399
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Trp(p.R259W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000437212
Start	118107856:118107856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript