Colon Cancer: Gene >> IGF2BP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185649496:185649496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500C>A
AA Mutation	p.Asn500Lys(p.N500K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185824820:185824820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>G
AA Mutation	p.Asp47Glu(p.D47E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185675347:185675347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020G>C
AA Mutation	p.Glu340Asp(p.E340D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185672633:185672633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200027200
CDS Mutation	c.1108G>A
AA Mutation	p.Ala370Thr(p.A370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185649461:185649461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528084524
CDS Mutation	c.1535C>T
AA Mutation	p.Ala512Val(p.A512V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382199
Start	185689609:185689609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563013811
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382199
Start	185658353:185658353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151111656
CDS Mutation	c.1257G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IGF2BP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185647036:185647036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696T>G
AA Mutation	p.Phe566Val(p.F566V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382199
Start	185824866:185824866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95G>A
AA Mutation	p.Gly32Glu(p.G32E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000382199
Start	185658340:185658340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript