Colon Cancer: Gene >> DLL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40931706:40931706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598T>C
AA Mutation	p.Cys200Arg(p.C200R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40936444:40936444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779386236
CDS Mutation	c.1457C>T
AA Mutation	p.Ser486Leu(p.S486L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40934710:40934710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013G>A
AA Mutation	p.Ser338Asn(p.S338N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40936653:40936653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369740396
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Trp(p.R556W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40936308:40936308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374162819
CDS Mutation	c.1321G>A
AA Mutation	p.Val441Ile(p.V441I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249749
Start	40937523:40937523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2049G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249749
Start	40936913:40936913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750012148
CDS Mutation	c.1926G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249749
Start	40934664:40934664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DLL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249749
Start	40936335:40936335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755422423
CDS Mutation	c.1348G>A
AA Mutation	p.Ala450Thr(p.A450T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript