Colon Cancer: Gene >> PRKCZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2172058:2172058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1065C>A
AA Mutation	p.Phe355Leu(p.F355L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2184975:2184975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745A>G
AA Mutation	p.Asn582Ser(p.N582S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2150814:2150814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712A>G
AA Mutation	p.Met238Val(p.M238V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2059568:2059568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>T
AA Mutation	p.Gly104Val(p.G104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378567
Start	2150876:2150876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375972106
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378567
Start	2055474:2055474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378567
Start	2144230:2144230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378567
Start	2150972:2150972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378567
Start	2175283:2175283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371504744
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000378567
Start	2059541:2059541(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.287delT
AA Mutation	p.Phe96SerfsTer83(p.F96Sfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378567
Start	2150886:2150886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.784delA
AA Mutation	p.Ser262AlafsTer10(p.S262Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000378567
Start	2184700:2184700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1691+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRKCZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2146093:2146093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745674432
CDS Mutation	c.619G>A
AA Mutation	p.Glu207Lys(p.E207K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378567
Start	2172062:2172062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069G>A
AA Mutation	p.Ala357Thr(p.A357T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript