Colon Cancer: Gene >> PLK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23680974:23680974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>T
AA Mutation	p.Gly213Val(p.G213V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23684008:23684008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955C>A
AA Mutation	p.Leu319Met(p.L319M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689337:23689337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1370A>G
AA Mutation	p.Asp457Gly(p.D457G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689654:23689654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586G>A
AA Mutation	p.Ser529Asn(p.S529N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689939:23689939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748564084
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563His(p.R563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689987:23689987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736G>A
AA Mutation	p.Arg579Gln(p.R579Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23680932:23680932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596C>T
AA Mutation	p.Thr199Ile(p.T199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689920:23689920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Trp(p.R557W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689593:23689593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525C>T
AA Mutation	p.Pro509Ser(p.P509S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689352:23689352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1385A>G
AA Mutation	p.Tyr462Cys(p.Y462C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23683930:23683930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23681026:23681026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23690006:23690006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1755T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23680996:23680996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747697585
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300093
Start	23687502:23687502(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1074delA
AA Mutation	p.Glu359LysfsTer96(p.E359Kfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000300093
Start	23687522:23687522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Ter(p.R364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000300093
Start	23680180:23680180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Ter(p.R169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300093
Start	23689508:23689509(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1441_1442insTT
AA Mutation	p.Tyr481PhefsTer7(p.Y481Ffs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PLK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23679261:23679261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329A>G
AA Mutation	p.His110Arg(p.H110R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23680181:23680181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23684030:23684030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749527952
CDS Mutation	c.977C>T
AA Mutation	p.Ser326Leu(p.S326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000300093
Start	23688717:23688717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1242G>A
AA Mutation	p.Trp414Ter(p.W414*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript