Colon Cancer: Gene >> PKN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14441302:14441302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763268558
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Trp(p.R61W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14469351:14469351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987G>A
AA Mutation	p.Glu663Lys(p.E663K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14464122:14464122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1700C>T
AA Mutation	p.Ser567Leu(p.S567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14458079:14458079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214C>T
AA Mutation	p.Thr405Met(p.T405M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14463842:14463842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144549826
CDS Mutation	c.1510C>T
AA Mutation	p.Arg504Cys(p.R504C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14463960:14463960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369267115
CDS Mutation	c.1628G>A
AA Mutation	p.Arg543Gln(p.R543Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14464092:14464092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670C>T
AA Mutation	p.Thr557Ile(p.T557I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14441267:14441267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146A>C
AA Mutation	p.Glu49Ala(p.E49A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14469511:14469511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2147G>A
AA Mutation	p.Arg716His(p.R716H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000242783
Start	14470849:14470849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2623A>G
AA Mutation	p.Arg875Gly(p.R875G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14471636:14471636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746308814
CDS Mutation	c.2681C>T
AA Mutation	p.Thr894Met(p.T894M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14470238:14470238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372869100
CDS Mutation	c.2369C>T
AA Mutation	p.Thr790Met(p.T790M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14450411:14450411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704T>A
AA Mutation	p.Val235Glu(p.V235E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000242783
Start	14470850:14470850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2624G>T
AA Mutation	p.Arg875Met(p.R875M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14470201:14470201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332A>G
AA Mutation	p.Thr778Ala(p.T778A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14443491:14443491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371928270
CDS Mutation	c.344C>T
AA Mutation	p.Ala115Val(p.A115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14463854:14463854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522A>T
AA Mutation	p.Met508Leu(p.M508L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242783
Start	14463835:14463835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149310057
CDS Mutation	c.1503G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242783
Start	14451030:14451030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242783
Start	14441412:14441412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242783
Start	14471760:14471760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2805C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242783
Start	14469390:14469391(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2026_2027insG
AA Mutation	p.Pro676ArgfsTer39(p.P676Rfs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PKN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14446508:14446508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242783
Start	14450912:14450912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773C>T
AA Mutation	p.Thr258Ile(p.T258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript