Colon Cancer: Gene >> DCLK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737654:36737654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373984062
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Trp(p.R336W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737675:36737675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>T
AA Mutation	p.Pro329Ser(p.P329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36738562:36738562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373966326
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36738305:36738305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737798:36737798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181512442
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36738619:36738619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737581:36737581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34416671
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360Gln(p.R360Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36738631:36738631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>T
AA Mutation	p.Ser10Ile(p.S10I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737970:36737970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690G>T
AA Mutation	p.Glu230Asp(p.E230D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36715464:36715464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1811C>T
AA Mutation	p.Ala604Val(p.A604V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36718143:36718143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771625779
CDS Mutation	c.1620C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36718095:36718095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36737310:36737310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528794239
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36737220:36737220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116865058
CDS Mutation	c.1440G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36738294:36738294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36738615:36738615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416516
Start	36738333:36738333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.327delC
AA Mutation	p.Arg110GlyfsTer69(p.R110Gfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416516
Start	36738365:36738366(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.294dupG
AA Mutation	p.Lys99GlufsTer8(p.K99Efs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DCLK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416516
Start	36737928:36737928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732G>T
AA Mutation	p.Lys244Asn(p.K244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36715388:36715388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1887C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36715409:36715409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1866G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36738306:36738306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552055548
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416516
Start	36721531:36721531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000416516
Start	36738272:36738272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>T
AA Mutation	p.Glu130Ter(p.E130*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript