Colon Cancer: Gene >> KLF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56265408:56265408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>A
AA Mutation	p.Leu104Ile(p.L104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284390:56284390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976C>T
AA Mutation	p.Arg326Cys(p.R326C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284475:56284475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061G>A
AA Mutation	p.Arg354His(p.R354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284453:56284453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1039G>C
AA Mutation	p.Asp347His(p.D347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284468:56284468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054C>T
AA Mutation	p.His352Tyr(p.H352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284478:56284478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284351:56284351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937T>A
AA Mutation	p.Trp313Arg(p.W313R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56265261:56265261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163A>G
AA Mutation	p.Asn55Asp(p.N55D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56284364:56284364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950G>A
AA Mutation	p.Arg317His(p.R317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000468660
Start	56233341:56233341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Asp3Asn(p.D3N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468660
Start	56270218:56270218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146271748
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000468660
Start	56265513:56265513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000468660
Start	56270255:56270255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832T>G
AA Mutation	p.Phe278Val(p.F278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript