Colon Cancer: Gene >> GGA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23467691:23467691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Cys(p.R581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23480741:23480741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910A>G
AA Mutation	p.Thr304Ala(p.T304A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23482970:23482970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751749491
CDS Mutation	c.833C>T
AA Mutation	p.Thr278Met(p.T278M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309859
Start	23480770:23480770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146363257
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23486056:23486056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>G
AA Mutation	p.Arg253Gly(p.R253G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309859
Start	23491799:23491799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353A>G
AA Mutation	p.Tyr118Cys(p.Y118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23493386:23493386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309859
Start	23495702:23495702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000309859
Start	23486732:23486732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638T>G
AA Mutation	p.Leu213Ter(p.L213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000309859
Start	23491707:23491707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774194384
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Ter(p.R149*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000309859
Start	23493459:23493459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000309859
Start	23486153:23486154(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.661-2dupA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GGA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309859
Start	23470129:23470129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760553146
CDS Mutation	c.1487G>T
AA Mutation	p.Gly496Val(p.G496V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309859
Start	23486725:23486725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript