Colon Cancer: Gene >> CEBPZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37228081:37228081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112A>G
AA Mutation	p.Glu371Gly(p.E371G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37231519:37231519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37228834:37228834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359T>C
AA Mutation	p.Ile120Thr(p.I120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37227547:37227547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143633668
CDS Mutation	c.1646A>G
AA Mutation	p.Tyr549Cys(p.Y549C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37216391:37216391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2236C>T
AA Mutation	p.Pro746Ser(p.P746S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37216354:37216354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552370367
CDS Mutation	c.2273G>A
AA Mutation	p.Arg758Gln(p.R758Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000234170
Start	37223171:37223171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145996359
CDS Mutation	c.1880C>T
AA Mutation	p.Pro627Leu(p.P627L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37227571:37227571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622C>T
AA Mutation	p.Ser541Leu(p.S541L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37228793:37228793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400A>G
AA Mutation	p.Thr134Ala(p.T134A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37216188:37216188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2332A>G
AA Mutation	p.Met778Val(p.M778V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37228721:37228721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472A>G
AA Mutation	p.Lys158Glu(p.K158E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234170
Start	37228359:37228359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141438261
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234170
Start	37212036:37212036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768774611
CDS Mutation	c.2607C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234170
Start	37228707:37228707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234170
Start	37228923:37228923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762499091
CDS Mutation	c.270T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000234170
Start	37228622:37228622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>T
AA Mutation	p.Glu191Ter(p.E191*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000234170
Start	37228844:37228844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>T
AA Mutation	p.Glu117Ter(p.E117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CEBPZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234170
Start	37220402:37220402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2137C>A
AA Mutation	p.Leu713Ile(p.L713I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript