Colon Cancer: Gene >> ZBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57611874:57611874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Gly243Arg(p.G243R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57610337:57610337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147660947
CDS Mutation	c.905C>T
AA Mutation	p.Ser302Leu(p.S302L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57615034:57615034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>T
AA Mutation	p.Asp119Tyr(p.D119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57615016:57615016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373G>A
AA Mutation	p.Ala125Thr(p.A125T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57614997:57614997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392C>T
AA Mutation	p.Ala131Val(p.A131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57604755:57604755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Asp370Asn(p.D370N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57611813:57611813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788G>T
AA Mutation	p.Arg263Leu(p.R263L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57614977:57614977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412A>G
AA Mutation	p.Lys138Glu(p.K138E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371173
Start	57610288:57610288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146958594
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371173
Start	57610336:57610336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374383138
CDS Mutation	c.906G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371173
Start	57611857:57611857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000371173
Start	57614965:57614965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754746401
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Ter(p.R142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000371173
Start	57604587:57604587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>T
AA Mutation	p.Gly426Ter(p.G426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000371173
Start	57613331:57613331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZBP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371173
Start	57604767:57604767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141295310
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Cys(p.R366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57615018:57615018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>T
AA Mutation	p.Arg124Met(p.R124M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371173
Start	57610307:57610307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935C>A
AA Mutation	p.Thr312Asn(p.T312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371173
Start	57610264:57610264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143130163
CDS Mutation	c.978G>A
Mutation Classification	Silent
Feature Type	Transcript