Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AKT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243505256:243505256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751275167
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478Gln(p.R478Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243637703:243637703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>T
AA Mutation	p.Gly157Cys(p.G157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243695654:243695654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Gly37Arg(p.G37R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263826
Start	243843127:243843127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44G>T
AA Mutation	p.Arg15Met(p.R15M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243572952:243572952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772090769
CDS Mutation	c.793G>A
AA Mutation	p.Gly265Arg(p.G265R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243552836:243552836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056G>T
AA Mutation	p.Glu352Asp(p.E352D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243552835:243552835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057A>C
AA Mutation	p.Lys353Gln(p.K353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243637691:243637691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481A>G
AA Mutation	p.Lys161Glu(p.K161E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263826
Start	243552920:243552920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263826
Start	243552859:243552860(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1032_1033insTTTGGAT
AA Mutation	p.Pro345PhefsTer10(p.P345Ffs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263826
Start	243505335:243505335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AKT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243505256:243505256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751275167
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478Gln(p.R478Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263826
Start	243645897:243645897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425G>T
AA Mutation	p.Arg142Ile(p.R142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000263826
Start	243646033:243646033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>T
AA Mutation	p.Glu97Ter(p.E97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript