Colon Cancer: Gene >> LMNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126819018:126819018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036A>C
AA Mutation	p.Met346Leu(p.M346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126826097:126826097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1601C>A
AA Mutation	p.Ser534Tyr(p.S534Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126818994:126818994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012A>G
AA Mutation	p.Met338Val(p.M338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126804847:126804847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431C>T
AA Mutation	p.Ser144Leu(p.S144L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126805604:126805604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550T>G
AA Mutation	p.Leu184Val(p.L184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126804885:126804885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469A>C
AA Mutation	p.Lys157Gln(p.K157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126811816:126811816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857T>C
AA Mutation	p.Val286Ala(p.V286A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261366
Start	126819047:126819047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261366
Start	126819023:126819023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202037109
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261366
Start	126819008:126819009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1035_1036delGA
AA Mutation	p.Glu345AspfsTer14(p.E345Dfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261366
Start	126805594:126805595(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.546dupA
AA Mutation	p.Gln183ThrfsTer5(p.Q183Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LMNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126826089:126826089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593G>T
AA Mutation	p.Leu531Phe(p.L531F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126819132:126819132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150G>A
AA Mutation	p.Glu384Lys(p.E384K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261366
Start	126818992:126818992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261366
Start	126810212:126810212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375453322
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261366
Start	126804881:126804882(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.472dupA
AA Mutation	p.Ser158LysfsTer30(p.S158Kfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript