Colon Cancer: Gene >> EPHB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100817204:100817204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576A>C
AA Mutation	p.Thr526Pro(p.T526P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100820158:100820158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100820273:100820273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832C>T
AA Mutation	p.Pro278Ser(p.P278S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100819734:100819734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534368922
CDS Mutation	c.1120G>A
AA Mutation	p.Gly374Arg(p.G374R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100805589:100805589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769965440
CDS Mutation	c.2590C>T
AA Mutation	p.Arg864Trp(p.R864W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100805513:100805513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146445434
CDS Mutation	c.2666G>A
AA Mutation	p.Arg889Gln(p.R889Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100813702:100813702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706G>A
AA Mutation	p.Gly569Glu(p.G569E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100823817:100823817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774048106
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Trp(p.R80W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100820170:100820170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765819602
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100823678:100823678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377T>G
AA Mutation	p.Leu126Arg(p.L126R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358173
Start	100805192:100805192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567264878
CDS Mutation	c.2808C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358173
Start	100812876:100812876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358173
Start	100823695:100823695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377679562
CDS Mutation	c.360G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EPHB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100822585:100822585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758697441
CDS Mutation	c.494G>A
AA Mutation	p.Arg165His(p.R165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100803545:100803545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2880A>C
AA Mutation	p.Lys960Asn(p.K960N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358173
Start	100813684:100813684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs60537976
CDS Mutation	c.1724C>T
AA Mutation	p.Ser575Leu(p.S575L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358173
Start	100820190:100820190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139571805
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript