Mutation

Primary Site >> Stomach Cancer

Gene >> AGO2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140557105:140557105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010C>G
AA Mutation	p.Thr337Ser(p.T337S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140551393:140551393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438Gln(p.R438Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140551328:140551328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Arg460Cys(p.R460C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140532471:140532471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>A
AA Mutation	p.Ala806Thr(p.A806T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140555904:140555904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>A
AA Mutation	p.Gly421Arg(p.G421R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140585234:140585234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100T>C
AA Mutation	p.Ser34Pro(p.S34P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140549125:140549125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760059271
CDS Mutation	c.1577C>T
AA Mutation	p.Thr526Met(p.T526M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140539346:140539346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2143C>T
AA Mutation	p.Leu715Phe(p.L715F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140557171:140557171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>T
AA Mutation	p.Arg315Met(p.R315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140541319:140541319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879G>A
AA Mutation	p.Ala627Thr(p.A627T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000220592
Start	140560473:140560473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764154303
CDS Mutation	c.556G>A
AA Mutation	p.Glu186Lys(p.E186K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140560477:140560477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144947708
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140555944:140555944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747025316
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140551344:140551344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749725024
CDS Mutation	c.1362G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140585232:140585232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781495805
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140532107:140532107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2517C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140532577:140532577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751186251
CDS Mutation	c.2310C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140551338:140551338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267601798
CDS Mutation	c.1368C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140535501:140535501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2238C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140541197:140541197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220592
Start	140555905:140555905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560546827
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140551331:140551331(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1375delC
AA Mutation	p.Gln459SerfsTer9(p.Q459Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140549210:140549210(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1492delG
AA Mutation	p.Ala498ArgfsTer11(p.A498Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220592
Start	140547593:140547593(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1623delG
AA Mutation	p.Met542TrpfsTer8(p.M542Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript