Mutation

Primary Site >> Stomach Cancer

Gene >> TLR4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713444:117713444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316A>T
AA Mutation	p.Glu439Val(p.E439V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712625:117712625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497A>C
AA Mutation	p.Lys166Thr(p.K166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713721:117713721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1593C>A
AA Mutation	p.Asn531Lys(p.N531K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713620:117713620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492T>G
AA Mutation	p.Leu498Val(p.L498V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713638:117713638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510T>C
AA Mutation	p.Ser504Pro(p.S504P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713983:117713983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855C>T
AA Mutation	p.Pro619Ser(p.P619S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712940:117712940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812A>C
AA Mutation	p.Lys271Thr(p.K271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712756:117712756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>A
AA Mutation	p.Leu210Met(p.L210M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712711:117712711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583T>G
AA Mutation	p.Leu195Val(p.L195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712634:117712634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506A>T
AA Mutation	p.Glu169Val(p.E169V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712463:117712463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335A>G
AA Mutation	p.Asn112Ser(p.N112S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714074:117714074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1946T>G
AA Mutation	p.Val649Gly(p.V649G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713510:117713510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382T>G
AA Mutation	p.Val461Gly(p.V461G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713435:117713435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307A>G
AA Mutation	p.Gln436Arg(p.Q436R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713446:117713446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318T>G
AA Mutation	p.Phe440Val(p.F440V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714484:117714484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2356T>C
AA Mutation	p.Tyr786His(p.Y786H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713285:117713285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157G>A
AA Mutation	p.Ser386Asn(p.S386N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713587:117713587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459T>G
AA Mutation	p.Phe487Val(p.F487V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712768:117712768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>G
AA Mutation	p.Pro214Ala(p.P214A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712689:117712689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561T>G
AA Mutation	p.Ile187Met(p.I187M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713444:117713444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316A>C
AA Mutation	p.Glu439Ala(p.E439A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713585:117713585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1457A>C
AA Mutation	p.Asn486Thr(p.N486T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714259:117714259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131G>T
AA Mutation	p.Asp711Tyr(p.D711Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117712632:117712632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745563363
CDS Mutation	c.504T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117712965:117712965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117714570:117714570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117713880:117713880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355622
Start	117713806:117713806(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1683delA
AA Mutation	p.Lys561AsnfsTer11(p.K561Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript