Colon Cancer: Gene >> AGO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35853546:35853546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2527G>A
AA Mutation	p.Ala843Thr(p.A843T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373210
Start	35832183:35832183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Trp(p.R415W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35831839:35831839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024T>A
AA Mutation	p.Cys342Ser(p.C342S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35841287:35841287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754880287
CDS Mutation	c.1847G>A
AA Mutation	p.Arg616Gln(p.R616Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35841319:35841319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369348803
CDS Mutation	c.1879C>T
AA Mutation	p.Arg627Trp(p.R627W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35816888:35816888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769017079
CDS Mutation	c.26C>T
AA Mutation	p.Pro9Leu(p.P9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35841286:35841286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751529574
CDS Mutation	c.1846C>T
AA Mutation	p.Arg616Trp(p.R616W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35850887:35850887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2311T>G
AA Mutation	p.Trp771Gly(p.W771G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35834099:35834099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489T>C
AA Mutation	p.Phe497Leu(p.F497L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35816990:35816990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>T
AA Mutation	p.Asp43Val(p.D43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35841434:35841434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1994G>A
AA Mutation	p.Arg665Gln(p.R665Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373210
Start	35825930:35825930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373210
Start	35841744:35841745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2170_2171delGA
AA Mutation	p.Glu724LysfsTer16(p.E724Kfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373210
Start	35817023:35817023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.165delA
AA Mutation	p.Lys55AsnfsTer10(p.K55Nfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000373210
Start	35816947:35816947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Ter(p.R29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35841355:35841355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1915G>A
AA Mutation	p.Glu639Lys(p.E639K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35826787:35826787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373210
Start	35850251:35850251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2270G>T
AA Mutation	p.Gly757Val(p.G757V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000373210
Start	35816947:35816947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Ter(p.R29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript