Colon Cancer: Gene >> DLL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205143
Start	39507928:39507928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1772T>C
AA Mutation	p.Leu591Pro(p.L591P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205143
Start	39505327:39505327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139638161
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205143
Start	39504255:39504255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200850430
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205143
Start	39507592:39507592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1647G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205143
Start	39507854:39507854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1698T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205143
Start	39507923:39507923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000205143
Start	39507932:39507932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776323833
CDS Mutation	c.1781delC
AA Mutation	p.Pro594ArgfsTer24(p.P594Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000205143
Start	39504130:39504130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894675
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Ter(p.R238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DLL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205143
Start	39507883:39507883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727T>C
AA Mutation	p.Val576Ala(p.V576A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript