Colon Cancer: Gene >> LIN9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226286358:226286358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Trp(p.R183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226232592:226232592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1586A>C
AA Mutation	p.Asn529Thr(p.N529T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226266281:226266281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226250846:226250846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160A>C
AA Mutation	p.Glu387Ala(p.E387A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328205
Start	226266321:226266321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328205
Start	226232519:226232519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LIN9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226266251:226266251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761143720
CDS Mutation	c.946C>T
AA Mutation	p.Arg316Trp(p.R316W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript