Colon Cancer: Gene >> REM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31484276:31484276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779674989
CDS Mutation	c.743G>C
AA Mutation	p.Arg248Pro(p.R248P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31484165:31484165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632G>A
AA Mutation	p.Arg211His(p.R211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31482465:31482465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199660041
CDS Mutation	c.602G>A
AA Mutation	p.Arg201His(p.R201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31477852:31477852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749761528
CDS Mutation	c.365C>T
AA Mutation	p.Thr122Met(p.T122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31482401:31482401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751705132
CDS Mutation	c.538C>T
AA Mutation	p.Arg180Trp(p.R180W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000201979
Start	31482319:31482319(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.461delG
AA Mutation	p.Gly154AlafsTer111(p.G154Afs*111)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000201979
Start	31477911:31477911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772122529
CDS Mutation	c.423+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> REM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000201979
Start	31482428:31482428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>T
AA Mutation	p.Pro189Ser(p.P189S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript