Colon Cancer: Gene >> AGO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35919537:35919537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2504G>A
AA Mutation	p.Arg835Gln(p.R835Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35893182:35893182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748561732
CDS Mutation	c.416G>A
AA Mutation	p.Arg139Gln(p.R139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35914221:35914221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780G>A
AA Mutation	p.Ala594Thr(p.A594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373204
Start	35892675:35892675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Trp(p.R110W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35907018:35907018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481A>G
AA Mutation	p.Gln494Arg(p.Q494R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35893741:35893741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580C>T
AA Mutation	p.Arg194Cys(p.R194C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35919588:35919588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2555G>A
AA Mutation	p.Arg852His(p.R852H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35895222:35895222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973T>C
AA Mutation	p.Cys325Arg(p.C325R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35894362:35894362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Cys(p.R278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35892672:35892672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371043471
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373204
Start	35901533:35901533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199616208
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373204
Start	35915413:35915413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1899G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000373204
Start	35915510:35915510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Ter(p.R666*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35893137:35893137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371G>T
AA Mutation	p.Arg124Leu(p.R124L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373204
Start	35888551:35888551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200988923
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373204
Start	35919601:35919601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764523718
CDS Mutation	c.2568C>T
Mutation Classification	Silent
Feature Type	Transcript