Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DUSP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73769272:73769272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628A>C
AA Mutation	p.Ile210Leu(p.I210L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73780061:73780061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55T>C
AA Mutation	p.Cys19Arg(p.C19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73766460:73766460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754738933
CDS Mutation	c.893G>A
AA Mutation	p.Arg298Gln(p.R298Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73779970:73779970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Ser49Asn(p.S49N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272444
Start	73775000:73775000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272444
Start	73775008:73775008(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762094663
CDS Mutation	c.355delT
AA Mutation	p.Ser119ProfsTer18(p.S119Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73769319:73769319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581T>G
AA Mutation	p.Leu194Arg(p.L194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272444
Start	73773858:73773858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516G>T
AA Mutation	p.Glu172Asp(p.E172D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272444
Start	73780074:73780074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376117582
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript