Colon Cancer: Gene >> RBPMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320203
Start	30544545:30544545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>T
AA Mutation	p.Pro150Leu(p.P150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320203
Start	30504420:30504420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381C>A
AA Mutation	p.Phe127Leu(p.F127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320203
Start	30558890:30558890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000320203
Start	30504430:30504430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>T
AA Mutation	p.Glu131Ter(p.E131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000320203
Start	30385160:30385160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RBPMS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320203
Start	30544607:30544607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Ala171Thr(p.A171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000320203
Start	30504430:30504430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>T
AA Mutation	p.Glu131Ter(p.E131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript