Colon Cancer: Gene >> IGFBP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269593
Start	40456479:40456479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673A>G
AA Mutation	p.Lys225Glu(p.K225E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269593
Start	40454037:40454037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>A
AA Mutation	p.Arg206His(p.R206H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269593
Start	40456546:40456546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740T>G
AA Mutation	p.Leu247Arg(p.L247R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269593
Start	40453117:40453117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745961147
CDS Mutation	c.482C>T
AA Mutation	p.Ala161Val(p.A161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269593
Start	40443852:40443852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778799414
CDS Mutation	c.123delC
AA Mutation	p.Val42TrpfsTer52(p.V42Wfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000269593
Start	40454060:40454060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640C>T
AA Mutation	p.Gln214Ter(p.Q214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IGFBP4

No Mutation Annotation!