Colon Cancer: Gene >> RBM47

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40437888:40437888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Ala336Thr(p.A336T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40438013:40438013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40436563:40436563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208C>T
AA Mutation	p.Ala403Val(p.A403V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40437813:40437813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081T>C
AA Mutation	p.Tyr361His(p.Y361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40438481:40438481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774218691
CDS Mutation	c.413C>T
AA Mutation	p.Pro138Leu(p.P138L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40438143:40438143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40438425:40438425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Gly157Arg(p.G157R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295971
Start	40438654:40438654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199723210
CDS Mutation	c.240C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295971
Start	40436572:40436572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1199delG
AA Mutation	p.Gly400AspfsTer45(p.G400Dfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RBM47

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295971
Start	40438518:40438518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201192048
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Cys(p.R126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295971
Start	40438414:40438414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript