Colon Cancer: Gene >> PRKCI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170280353:170280353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Cys(p.R278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170295931:170295931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Cys(p.R480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000295797
Start	170295911:170295911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1418T>C
AA Mutation	p.Val473Ala(p.V473A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170263400:170263400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170293466:170293466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375T>C
AA Mutation	p.Ser459Pro(p.S459P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170295941:170295941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483His(p.R483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170222730:170222730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61G>T
AA Mutation	p.Asp21Tyr(p.D21Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170267983:170267983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295797
Start	170235314:170235314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140807328
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295797
Start	170291865:170291865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767492700
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295797
Start	170280339:170280340(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756514123
CDS Mutation	c.826dupA
AA Mutation	p.Thr276AsnfsTer16(p.T276Nfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000295797
Start	170280226:170280226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRKCI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170295932:170295932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480His(p.R480H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170284511:170284511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118G>T
AA Mutation	p.Gly373Val(p.G373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170281950:170281950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049T>G
AA Mutation	p.Leu350Arg(p.L350R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170291861:170291861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211T>C
AA Mutation	p.Leu404Ser(p.L404S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295797
Start	170303072:170303072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736T>G
AA Mutation	p.Phe579Cys(p.F579C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript