Colon Cancer: Gene >> TLK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62578515:62578515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293A>C
AA Mutation	p.Glu431Asp(p.E431D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62612540:62612540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146155200
CDS Mutation	c.2294C>T
AA Mutation	p.Ala765Val(p.A765V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62553744:62553744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709G>T
AA Mutation	p.Asp237Tyr(p.D237Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62612530:62612530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284A>G
AA Mutation	p.Thr762Ala(p.T762A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62573331:62573331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085A>G
AA Mutation	p.Gln362Arg(p.Q362R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62573218:62573218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972A>T
AA Mutation	p.Gln324His(p.Q324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62536306:62536306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Arg167Lys(p.R167K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62600722:62600722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688C>T
AA Mutation	p.Ser563Leu(p.S563L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62612420:62612420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769484053
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725Gln(p.R725Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326270
Start	62524253:62524253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326270
Start	62553679:62553679(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.649delA
AA Mutation	p.Ile217TyrfsTer4(p.I217Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000326270
Start	62573252:62573252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>T
AA Mutation	p.Glu336Ter(p.E336*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TLK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62602069:62602069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1814C>T
AA Mutation	p.Ala605Val(p.A605V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62553707:62553707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>T
AA Mutation	p.Lys224Asn(p.K224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326270
Start	62600736:62600736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Trp(p.R568W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript