Colon Cancer: Gene >> KLF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73061892:73061892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293C>G
AA Mutation	p.Pro98Arg(p.P98R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73062531:73062531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>T
AA Mutation	p.Ser311Ile(p.S311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73062518:73062518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919T>G
AA Mutation	p.Ser307Ala(p.S307A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73062020:73062020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750391044
CDS Mutation	c.421C>T
AA Mutation	p.Pro141Ser(p.P141S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73062623:73062623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024A>T
AA Mutation	p.Asn342Tyr(p.N342Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377687
Start	73062019:73062019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377687
Start	73061968:73061968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377687
Start	73075829:73075829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000377687
Start	73062528:73062530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.930_932delAAG
AA Mutation	p.Ser311del(p.S311del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73061921:73061921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Glu108Lys(p.E108K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377687
Start	73062510:73062510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911C>T
AA Mutation	p.Pro304Leu(p.P304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377687
Start	73062289:73062289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.690delG
AA Mutation	p.Gln230HisfsTer3(p.Q230Hfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript