Colon Cancer: Gene >> LMNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325327
Start	2435056:2435056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800A>G
AA Mutation	p.His267Arg(p.H267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325327
Start	2434020:2434020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367908162
CDS Mutation	c.1288C>T
AA Mutation	p.Arg430Cys(p.R430C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325327
Start	2438216:2438216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Cys(p.R211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325327
Start	2433931:2433931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749342900
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325327
Start	2456700:2456700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325327
Start	2431863:2431864(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs776267567
CDS Mutation	c.1629dupC
AA Mutation	p.Ser544LeufsTer23(p.S544Lfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000325327
Start	2430929:2430931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1843_1845delAGA
AA Mutation	p.Arg615del(p.R615del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LMNB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325327
Start	2432466:2432466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777408921
CDS Mutation	c.1540G>A
AA Mutation	p.Ala514Thr(p.A514T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript