Colon Cancer: Gene >> LIPG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49583682:49583682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284G>T
AA Mutation	p.Lys428Asn(p.K428N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49575563:49575563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750648857
CDS Mutation	c.766G>A
AA Mutation	p.Asp256Asn(p.D256N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49581639:49581639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018G>A
AA Mutation	p.Ala340Thr(p.A340T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49582424:49582424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099A>T
AA Mutation	p.Thr367Ser(p.T367S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49581580:49581580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959G>A
AA Mutation	p.Gly320Asp(p.G320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49569503:49569503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>A
AA Mutation	p.Gly176Arg(p.G176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49575411:49575411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614A>G
AA Mutation	p.His205Arg(p.H205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261292
Start	49569520:49569520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778959163
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261292
Start	49581461:49581461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LIPG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261292
Start	49583689:49583689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536799767
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Cys(p.R431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript