Colon Cancer: Gene >> RBM39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35732118:35732118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119G>A
AA Mutation	p.Ser40Asn(p.S40N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35729498:35729498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326G>A
AA Mutation	p.Arg109Gln(p.R109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35716801:35716801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830A>G
AA Mutation	p.Glu277Gly(p.E277G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35725084:35725084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488G>T
AA Mutation	p.Arg163Ile(p.R163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35714233:35714233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>T
AA Mutation	p.Asp350Tyr(p.D350Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RBM39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253363
Start	35714376:35714376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905A>G
AA Mutation	p.Glu302Gly(p.E302G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253363
Start	35716755:35716755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000253363
Start	35738981:35738981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88G>T
AA Mutation	p.Glu30Ter(p.E30*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript