Colon Cancer: Gene >> TAOK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29542672:29542672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2656G>T
AA Mutation	p.Gly886Cys(p.G886C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29495667:29495667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939G>T
AA Mutation	p.Lys313Asn(p.K313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29491798:29491798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764G>A
AA Mutation	p.Arg255His(p.R255H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29522319:29522319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1948G>A
AA Mutation	p.Ala650Thr(p.A650T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29467158:29467158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370461672
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29530554:29530554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772496224
CDS Mutation	c.2296C>T
AA Mutation	p.Arg766Trp(p.R766W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29491840:29491840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Arg269Gln(p.R269Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29522296:29522296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925A>G
AA Mutation	p.Gln642Arg(p.Q642R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29507972:29507972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415G>A
AA Mutation	p.Arg472Gln(p.R472Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29542928:29542928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772280663
CDS Mutation	c.2912G>A
AA Mutation	p.Arg971Gln(p.R971Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29478313:29478313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415T>A
AA Mutation	p.Leu139Ile(p.L139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261716
Start	29475687:29475687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000261716
Start	29534241:29534241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485C>T
AA Mutation	p.Arg829Ter(p.R829*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAOK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261716
Start	29475706:29475706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241C>G
AA Mutation	p.Gln81Glu(p.Q81E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript