Colon Cancer: Gene >> DCLK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150102514:150102514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766290066
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150102652:150102652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596T>G
AA Mutation	p.Val199Gly(p.V199G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150249574:150249574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963G>A
AA Mutation	p.Ala655Thr(p.A655T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150256096:150256096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150C>A
AA Mutation	p.Pro717His(p.P717H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150256242:150256242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2296G>A
AA Mutation	p.Asp766Asn(p.D766N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150193153:150193153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>T
AA Mutation	p.Asp258Tyr(p.D258Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150232406:150232406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1369G>A
AA Mutation	p.Glu457Lys(p.E457K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150079103:150079103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76G>T
AA Mutation	p.Gly26Trp(p.G26W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296550
Start	150247663:150247663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551849647
CDS Mutation	c.1839G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296550
Start	150239831:150239831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296550
Start	150232714:150232714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779339789
CDS Mutation	c.1452G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296550
Start	150249639:150249639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78390255
CDS Mutation	c.2028G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296550
Start	150256180:150256180(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs751255369
CDS Mutation	c.2239delC
AA Mutation	p.His747ThrfsTer153(p.H747Tfs*153)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296550
Start	150256156:150256156(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2214delC
AA Mutation	p.Thr739ProfsTer161(p.T739Pfs*161)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000296550
Start	150193213:150193213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832C>T
AA Mutation	p.Gln278Ter(p.Q278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296550
Start	150193155:150193156(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.780dupT
AA Mutation	p.Gly261TrpfsTer2(p.G261Wfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DCLK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150198023:150198023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881C>G
AA Mutation	p.Ser294Cys(p.S294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150256234:150256234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763His(p.R763H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150232688:150232688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426G>T
AA Mutation	p.Asp476Tyr(p.D476Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150232691:150232691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429C>A
AA Mutation	p.Leu477Ile(p.L477I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296550
Start	150239770:150239770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>A
AA Mutation	p.Ser532Tyr(p.S532Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296550
Start	150203838:150203838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776454680
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296550
Start	150256238:150256238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2293delC
AA Mutation	p.Arg765GlufsTer135(p.R765Efs*135)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000296550
Start	150193241:150193241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript