Colon Cancer: Gene >> RERG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256953
Start	15109180:15109180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>T
AA Mutation	p.Thr177Met(p.T177M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256953
Start	15109147:15109147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563A>G
AA Mutation	p.Gln188Arg(p.Q188R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256953
Start	15109174:15109174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746482571
CDS Mutation	c.536G>A
AA Mutation	p.Arg179Gln(p.R179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256953
Start	15109288:15109288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>T
AA Mutation	p.Ala141Val(p.A141V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256953
Start	15111373:15111373(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.163delT
AA Mutation	p.Ser55ProfsTer5(p.S55Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000256953
Start	15109295:15109295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>T
AA Mutation	p.Glu139Ter(p.E139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RERG

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000256953
Start	15109445:15109445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773343591
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Ter(p.R89*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript