Colon Cancer: Gene >> PI4KB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368873
Start	151315662:151315662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368873
Start	151315874:151315874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766903450
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368873
Start	151298952:151298952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1871A>C
AA Mutation	p.Lys624Thr(p.K624T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368873
Start	151315994:151315994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372795296
CDS Mutation	c.488G>A
AA Mutation	p.Arg163Gln(p.R163Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368873
Start	151292994:151292994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2309G>A
AA Mutation	p.Arg770Gln(p.R770Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368873
Start	151315879:151315879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368873
Start	151315894:151315894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368873
Start	151307610:151307610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1146C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368873
Start	151316287:151316287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201358714
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368873
Start	151303603:151303603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368873
Start	151316401:151316401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.81delG
AA Mutation	p.Ser28ProfsTer3(p.S28Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368873
Start	151316038:151316038(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.444delG
AA Mutation	p.Tyr149IlefsTer50(p.Y149Ifs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368873
Start	151315674:151315674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.808delA
AA Mutation	p.Arg270GlyfsTer14(p.R270Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000368873
Start	151301968:151301968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PI4KB

No Mutation Annotation!