Mutation

Primary Site >> Stomach Cancer

Gene >> TLR3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186083614:186083614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150315296
CDS Mutation	c.1928G>A
AA Mutation	p.Arg643His(p.R643H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186082867:186082867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141634515
CDS Mutation	c.1181G>A
AA Mutation	p.Arg394Gln(p.R394Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186082495:186082495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>A
AA Mutation	p.Gly270Glu(p.G270E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186082988:186082988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302A>C
AA Mutation	p.Glu434Asp(p.E434D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186076777:186076777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158T>C
AA Mutation	p.Ile53Thr(p.I53T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296795
Start	186084159:186084159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2473C>T
AA Mutation	p.Pro825Ser(p.P825S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296795
Start	186076658:186076658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369957478
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296795
Start	186076988:186076988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763487767
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296795
Start	186082865:186082865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296795
Start	186078956:186078956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296795
Start	186078995:186078995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.603delA
AA Mutation	p.Lys201AsnfsTer2(p.K201Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript