Colon Cancer: Gene >> AKT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40236044:40236044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021T>C
AA Mutation	p.Tyr341His(p.Y341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40235337:40235337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189C>T
AA Mutation	p.Pro397Ser(p.P397S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40237997:40237997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757245351
CDS Mutation	c.803C>T
AA Mutation	p.Ser268Leu(p.S268L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40242574:40242574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401A>G
AA Mutation	p.Glu134Gly(p.E134G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392038
Start	40242055:40242055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748740340
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392038
Start	40235139:40235139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392038
Start	40255241:40255241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139479466
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392038
Start	40238944:40238944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392038
Start	40238017:40238017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140472835
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000392038
Start	40235087:40235087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324G>T
AA Mutation	p.Glu442Ter(p.E442*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AKT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40240101:40240101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763319755
CDS Mutation	c.583G>A
AA Mutation	p.Ala195Thr(p.A195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392038
Start	40235093:40235093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>A
AA Mutation	p.Asp440Asn(p.D440N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000392038
Start	40265221:40265221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript