Colon Cancer: Gene >> GPAA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355091
Start	144083959:144083959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>T
AA Mutation	p.Asp179Tyr(p.D179Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355091
Start	144084810:144084810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Cys(p.R367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355091
Start	144083205:144083205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>C
AA Mutation	p.Glu52Asp(p.E52D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355091
Start	144084456:144084456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857G>T
AA Mutation	p.Gly286Val(p.G286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355091
Start	144085372:144085372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355091
Start	144085990:144085990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355091
Start	144084815:144084815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371058225
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355091
Start	144084451:144084451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPAA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355091
Start	144084497:144084497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782263637
CDS Mutation	c.898G>A
AA Mutation	p.Gly300Ser(p.G300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript