Colon Cancer: Gene >> MARK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63898238:63898238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751422215
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Cys(p.R99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63902259:63902259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63898817:63898817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63902286:63902286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767626610
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397His(p.R397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63902205:63902205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109G>A
AA Mutation	p.Gly370Asp(p.G370D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63900816:63900816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925G>A
AA Mutation	p.Glu309Lys(p.E309K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63902645:63902645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279A>G
AA Mutation	p.Thr427Ala(p.T427A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63904942:63904942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833G>T
AA Mutation	p.Leu611Phe(p.L611F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63895210:63895210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755618580
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Trp(p.R36W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63898611:63898611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341A>C
AA Mutation	p.Lys114Thr(p.K114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63900991:63900991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023G>T
AA Mutation	p.Glu341Asp(p.E341D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63901049:63901049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>A
AA Mutation	p.Leu361Met(p.L361M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63904141:63904141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670G>A
AA Mutation	p.Arg557Gln(p.R557Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402010
Start	63900056:63900056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.714T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402010
Start	63895278:63895278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402010
Start	63909072:63909072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402010
Start	63901042:63901042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402010
Start	63904791:63904791(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1687delC
AA Mutation	p.Gln563SerfsTer53(p.Q563Sfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402010
Start	63900012:63900012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.675delA
AA Mutation	p.Lys225AsnfsTer12(p.K225Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402010
Start	63904110:63904110(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1644delC
AA Mutation	p.Thr549ArgfsTer67(p.T549Rfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402010
Start	63898637:63898637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.370delA
AA Mutation	p.Thr124ArgfsTer18(p.T124Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MARK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402010
Start	63900603:63900603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813C>A
AA Mutation	p.Phe271Leu(p.F271L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402010
Start	63899942:63899942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript