Mutation

Primary Site >> Stomach Cancer

Gene >> AGO1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35919065:35919065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2276G>A
AA Mutation	p.Arg759Gln(p.R759Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35915480:35915480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1966C>A
AA Mutation	p.Arg656Ser(p.R656S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35893257:35893257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491T>C
AA Mutation	p.Met164Thr(p.M164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
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

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373204
Start	35902068:35902068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261C>T
AA Mutation	p.Arg421Trp(p.R421W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35888581:35888581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
AA Mutation	p.Lys60Asn(p.K60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35892609:35892609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774432228
CDS Mutation	c.262C>T
AA Mutation	p.Arg88Cys(p.R88C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373204
Start	35917594:35917594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2030T>A
AA Mutation	p.Ile677Lys(p.I677K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35913853:35913853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594C>T
AA Mutation	p.Arg532Cys(p.R532C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35902322:35902322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1382G>A
AA Mutation	p.Arg461Gln(p.R461Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373204
Start	35914272:35914272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756692838
CDS Mutation	c.1831G>A
AA Mutation	p.Ala611Thr(p.A611T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35917699:35917699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135G>A
AA Mutation	p.Arg712His(p.R712H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35915447:35915447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933C>T
AA Mutation	p.Arg645Cys(p.R645C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35919101:35919101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371456175
CDS Mutation	c.2312G>A
AA Mutation	p.Arg771His(p.R771H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35892670:35892670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323A>G
AA Mutation	p.Asn108Ser(p.N108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373204
Start	35902303:35902303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>A
AA Mutation	p.Ala455Thr(p.A455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373204
Start	35893755:35893755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373204
Start	35914235:35914235(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1799delC
AA Mutation	p.Pro600GlnfsTer14(p.P600Qfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript