Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KLF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73846247:73846247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250T>G
AA Mutation	p.Leu84Val(p.L84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73695543:73695543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156T>G
AA Mutation	p.Phe386Val(p.F386V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73695624:73695624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075G>A
AA Mutation	p.Ala359Thr(p.A359T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73695512:73695512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396His(p.R396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73846108:73846108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389T>C
AA Mutation	p.Ile130Thr(p.I130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000377669
Start	73764963:73764963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Ter(p.R282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73845863:73845863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375091947
CDS Mutation	c.634G>A
AA Mutation	p.Val212Met(p.V212M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377669
Start	73715400:73715400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995C>A
AA Mutation	p.Ser332Tyr(p.S332Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377669
Start	73846080:73846080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748128269
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript