Colon Cancer: Gene >> KLHL11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854560:41854560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307T>C
AA Mutation	p.Val436Ala(p.V436A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854849:41854849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018A>T
AA Mutation	p.Thr340Ser(p.T340S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41855086:41855086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>T
AA Mutation	p.Asp261Tyr(p.D261Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41855148:41855148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719A>G
AA Mutation	p.Glu240Gly(p.E240G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854326:41854326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782656916
CDS Mutation	c.1541G>A
AA Mutation	p.Arg514Gln(p.R514Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41853876:41853876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1991G>A
AA Mutation	p.Arg664Gln(p.R664Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854225:41854225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642T>G
AA Mutation	p.Phe548Val(p.F548V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854509:41854509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358G>T
AA Mutation	p.Gly453Val(p.G453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41854851:41854851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016G>A
AA Mutation	p.Gly339Asp(p.G339D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41855254:41855254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613T>G
AA Mutation	p.Cys205Gly(p.C205G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41865105:41865105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266G>A
AA Mutation	p.Arg89His(p.R89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319121
Start	41865176:41865176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319121
Start	41854511:41854511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1356A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319121
Start	41865174:41865174(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.197delC
AA Mutation	p.Pro66GlnfsTer92(p.P66Qfs*92)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319121
Start	41855018:41855019(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.848_849delGA
AA Mutation	p.Arg283IlefsTer3(p.R283Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319121
Start	41854280:41854281(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1586_1587delCA
AA Mutation	p.Thr529ArgfsTer15(p.T529Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319121
Start	41855017:41855018(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.848_849dupGA
AA Mutation	p.Tyr284AspfsTer15(p.Y284Dfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KLHL11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319121
Start	41855144:41855144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723T>G
AA Mutation	p.Phe241Leu(p.F241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript