Colon Cancer: Gene >> HMGB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296503
Start	173333102:173333102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263A>C
AA Mutation	p.Lys88Thr(p.K88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296503
Start	173332870:173332870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422A>G
AA Mutation	p.Lys141Arg(p.K141R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296503
Start	173333114:173333114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251A>T
AA Mutation	p.Asp84Val(p.D84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000296503
Start	173332869:173332870(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.422_423insCTG
AA Mutation	p.Lys141delinsAsnTer(p.K141delinsN*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HMGB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296503
Start	173332083:173332083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627A>T
AA Mutation	p.Glu209Asp(p.E209D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296503
Start	173333617:173333617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>A
Mutation Classification	Silent
Feature Type	Transcript