Colon Cancer: Gene >> ZER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128733457:128733457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212A>T
AA Mutation	p.Thr738Ser(p.T738S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128751447:128751447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004C>T
AA Mutation	p.Ser335Phe(p.S335F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000291900
Start	128750617:128750617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>T
AA Mutation	p.Thr453Met(p.T453M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128742596:128742596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509C>G
AA Mutation	p.Cys503Trp(p.C503W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128741563:128741563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1709G>A
AA Mutation	p.Gly570Asp(p.G570D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128733457:128733457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212A>G
AA Mutation	p.Thr738Ala(p.T738A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128739989:128739989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1984C>T
AA Mutation	p.Arg662Cys(p.R662C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128740064:128740064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780231279
CDS Mutation	c.1909G>A
AA Mutation	p.Val637Ile(p.V637I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128750770:128750770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760477266
CDS Mutation	c.1205A>G
AA Mutation	p.Lys402Arg(p.K402R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128753498:128753498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Gly138Ser(p.G138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128755557:128755557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202243417
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128753523:128753523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128753926:128753926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370841637
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128740837:128740837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769240282
CDS Mutation	c.1788G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128753559:128753559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140625501
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128753417:128753417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128741565:128741565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372057778
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128751134:128751134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291900
Start	128753526:128753526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000291900
Start	128752833:128752833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Ter(p.R255*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291900
Start	128735415:128735415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2059C>A
AA Mutation	p.Leu687Ile(p.L687I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript