Colon Cancer: Gene >> DLK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734327:100734327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767836232
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Trp(p.R195W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734592:100734592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848G>A
AA Mutation	p.Arg283His(p.R283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734487:100734487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749760314
CDS Mutation	c.743G>A
AA Mutation	p.Arg248His(p.R248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734282:100734282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734196:100734196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341267
Start	100732085:100732085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341267
Start	100734878:100734878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369392178
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341267
Start	100732121:100732121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341267
Start	100727110:100727110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341267
Start	100734218:100734218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.479delC
AA Mutation	p.Pro160LeufsTer50(p.P160Lfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DLK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341267
Start	100734508:100734508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764T>C
AA Mutation	p.Val255Ala(p.V255A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341267
Start	100729038:100729038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369997830
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript