Colon Cancer: Gene >> DRAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111118182:111118182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111124753:111124753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774377749
CDS Mutation	c.328G>A
AA Mutation	p.Ala110Thr(p.A110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111120659:111120659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374C>T
AA Mutation	p.Ala125Val(p.A125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111118260:111118260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>A
AA Mutation	p.Ser234Tyr(p.S234Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111120609:111120609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Leu142Phe(p.L142F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286692
Start	111124817:111124817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286692
Start	111131471:111131471(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.84delT
AA Mutation	p.Thr29LeufsTer3(p.T29Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DRAM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286692
Start	111126269:111126269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157A>G
AA Mutation	p.Lys53Glu(p.K53E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript