Colon Cancer: Gene >> AKT1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000349310
Start	104780214:104780214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121434592
CDS Mutation	c.49G>A
AA Mutation	p.Glu17Lys(p.E17K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104772900:104772900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150C>T
AA Mutation	p.Leu384Phe(p.L384F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104780120:104780120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774836044
CDS Mutation	c.143G>A
AA Mutation	p.Arg48His(p.R48H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000349310
Start	104776660:104776660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760536822
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104772942:104772942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549370342
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Cys(p.R370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104775726:104775726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369198922
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Trp(p.R121W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104776708:104776708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238T>C
AA Mutation	p.Trp80Arg(p.W80R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349310
Start	104774997:104774997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Val192Met(p.V192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349310
Start	104773921:104773921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767346459
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349310
Start	104773948:104773948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349310
Start	104773329:104773329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139200289
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349310
Start	104775145:104775145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AKT1

No Mutation Annotation!