Colon Cancer: Gene >> TNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195867771:195867771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552313951
CDS Mutation	c.2482G>A
AA Mutation	p.Ala828Thr(p.A828T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195888504:195888504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>T
AA Mutation	p.Asp29Tyr(p.D29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195882065:195882065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>T
AA Mutation	p.Lys291Asn(p.K291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195867728:195867728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2525C>T
AA Mutation	p.Pro842Leu(p.P842L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000333602
Start	195872277:195872277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755481543
CDS Mutation	c.1450G>A
AA Mutation	p.Glu484Lys(p.E484K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195884942:195884942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763489801
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195872451:195872451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Cys(p.R426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195882070:195882070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762033031
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Cys(p.R290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195882148:195882148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790G>A
AA Mutation	p.Asp264Asn(p.D264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195879165:195879165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747816316
CDS Mutation	c.898G>A
AA Mutation	p.Glu300Lys(p.E300K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333602
Start	195872398:195872398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333602
Start	195888532:195888532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333602
Start	195882086:195882086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146324948
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333602
Start	195882176:195882176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333602
Start	195870135:195870135(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757643410
CDS Mutation	c.1522delC
AA Mutation	p.Gln508SerfsTer3(p.Q508Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333602
Start	195867762:195867762(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2491delC
AA Mutation	p.Gln831ArgfsTer2(p.Q831Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333602
Start	195867591:195867591(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2662delC
AA Mutation	p.Leu888CysfsTer83(p.L888Cfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333602
Start	195870174:195870175(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779354232
CDS Mutation	c.1482dupC
AA Mutation	p.Asp495ArgfsTer25(p.D495Rfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000333602
Start	195883311:195883311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TNK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333602
Start	195879069:195879069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994A>G
AA Mutation	p.Ile332Val(p.I332V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333602
Start	195882086:195882086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146324948
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript