Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CBLL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107753480:107753480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251G>T
AA Mutation	p.Arg84Ile(p.R84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107759104:107759104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402G>T
AA Mutation	p.Gly468Cys(p.G468C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107758412:107758412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710A>G
AA Mutation	p.His237Arg(p.H237R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107748940:107748940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756843724
CDS Mutation	c.74G>A
AA Mutation	p.Arg25Gln(p.R25Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440859
Start	107758957:107758957(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1259delC
AA Mutation	p.Pro420LeufsTer20(p.P420Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBLL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107748985:107748985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781680484
CDS Mutation	c.119C>T
AA Mutation	p.Pro40Leu(p.P40L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440859
Start	107753417:107753417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188T>G
AA Mutation	p.Phe63Cys(p.F63C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440859
Start	107753451:107753452(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.227dupG
AA Mutation	p.Glu77Ter(p.E77*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript