Colon Cancer: Gene >> ASPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3481677:3481677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>G
AA Mutation	p.Asp104Gly(p.D104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3489304:3489304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596T>G
AA Mutation	p.Ile199Ser(p.I199S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3483533:3483533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754850338
CDS Mutation	c.467T>C
AA Mutation	p.Leu156Pro(p.L156P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3481702:3481702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336T>G
AA Mutation	p.Ile112Met(p.I112M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3481753:3481753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>T
AA Mutation	p.Glu129Asp(p.E129D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3481709:3481709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343C>A
AA Mutation	p.Leu115Ile(p.L115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263080
Start	3499071:3499071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755140673
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Cys(p.R309C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript