Colon Cancer: Gene >> TAOK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118244919:118244919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167C>A
AA Mutation	p.Ser56Tyr(p.S56Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118189916:118189916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753748348
CDS Mutation	c.1220C>T
AA Mutation	p.Ala407Val(p.A407V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118177222:118177222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1674T>G
AA Mutation	p.Ile558Met(p.I558M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118189811:118189811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325C>A
AA Mutation	p.Ser442Tyr(p.S442Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392533
Start	118199256:118199256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989A>G
AA Mutation	p.Asp330Gly(p.D330G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118199097:118199097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148A>G
AA Mutation	p.Asp383Gly(p.D383G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118199208:118199208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037G>A
AA Mutation	p.Ser346Asn(p.S346N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118233753:118233753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>T
AA Mutation	p.Glu188Asp(p.E188D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118172615:118172615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368702140
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Trp(p.R581W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118199062:118199062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373223808
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118172585:118172585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771C>T
AA Mutation	p.His591Tyr(p.H591Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392533
Start	118199221:118199221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>T
AA Mutation	p.Asp342Tyr(p.D342Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392533
Start	118152377:118152377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2385C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392533
Start	118151120:118151120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539247810
CDS Mutation	c.2574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392533
Start	118161982:118161982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000392533
Start	118181559:118181559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Gln460Ter(p.Q460*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392533
Start	118201351:118201352(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.931dupA
AA Mutation	p.Ile311AsnfsTer13(p.I311Nfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TAOK3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392533
Start	118160147:118160147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2351C>T
AA Mutation	p.Ala784Val(p.A784V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript