Colon Cancer: Gene >> CIZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128178901:128178901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306C>T
AA Mutation	p.His436Tyr(p.H436Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128178832:128178832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1375G>A
AA Mutation	p.Glu459Lys(p.E459K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128177672:128177672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370598569
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571His(p.R571H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128178960:128178960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247C>T
AA Mutation	p.Pro416Leu(p.P416L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128169477:128169477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767617433
CDS Mutation	c.2074C>T
AA Mutation	p.Arg692Cys(p.R692C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128185579:128185579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141376660
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Trp(p.R186W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128166394:128166394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2500G>A
AA Mutation	p.Ala834Thr(p.A834T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128185600:128185600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150582882
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Trp(p.R179W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128178473:128178473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516C>T
AA Mutation	p.Pro506Ser(p.P506S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128185638:128185638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497G>T
AA Mutation	p.Gly166Val(p.G166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128179074:128179074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133A>G
AA Mutation	p.Gln378Arg(p.Q378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372938
Start	128169486:128169486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139103399
CDS Mutation	c.2065G>A
AA Mutation	p.Val689Ile(p.V689I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372938
Start	128179280:128179280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372938
Start	128178749:128178749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201067611
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372938
Start	128166350:128166350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2544C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372938
Start	128166268:128166268(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2626delA
AA Mutation	p.Thr876HisfsTer5(p.T876Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000372938
Start	128169501:128169501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2050C>T
AA Mutation	p.Arg684Ter(p.R684*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CIZ1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000372938
Start	128169501:128169501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2050C>T
AA Mutation	p.Arg684Ter(p.R684*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript