Colon Cancer: Gene >> LNX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27567755:27567755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.740T>G
AA Mutation	p.Ile247Ser(p.I247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27562583:27562583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>T
AA Mutation	p.Gly352Cys(p.G352C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27569116:27569116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199501730
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Trp(p.R190W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27553419:27553419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567A>G
AA Mutation	p.Asn523Asp(p.N523D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27562681:27562681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.956G>A
AA Mutation	p.Arg319His(p.R319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27553304:27553304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540471303
CDS Mutation	c.1682C>T
AA Mutation	p.Ala561Val(p.A561V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316334
Start	27562518:27562518(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1119delG
AA Mutation	p.Leu374TrpfsTer8(p.L374Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000316334
Start	27562568:27562568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Ter(p.R357*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LNX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27569100:27569100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201989948
CDS Mutation	c.584C>T
AA Mutation	p.Ala195Val(p.A195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27553242:27553242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1744T>C
AA Mutation	p.Ser582Pro(p.S582P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316334
Start	27553217:27553217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1769G>C
AA Mutation	p.Gly590Ala(p.G590A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript