Mutation

Primary Site >> Stomach Cancer

Gene >> TLR8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12919362:12919362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>A
AA Mutation	p.Gly108Ser(p.G108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12921397:12921397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2357G>T
AA Mutation	p.Trp786Leu(p.W786L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12921084:12921084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2044A>G
AA Mutation	p.Thr682Ala(p.T682A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12919432:12919432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392T>C
AA Mutation	p.Leu131Pro(p.L131P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12920004:12920004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964T>G
AA Mutation	p.Tyr322Asp(p.Y322D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12921071:12921071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2031G>T
AA Mutation	p.Lys677Asn(p.K677N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12922125:12922125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085C>T
AA Mutation	p.Arg1029Trp(p.R1029W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12920455:12920455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1415G>A
AA Mutation	p.Arg472His(p.R472H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12919367:12919367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327A>G
AA Mutation	p.Ile109Met(p.I109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000218032
Start	12919686:12919686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Val216Met(p.V216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218032
Start	12921302:12921302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372127380
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218032
Start	12921917:12921917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2877T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218032
Start	12919841:12919841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218032
Start	12921757:12921757(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2718delA
AA Mutation	p.Glu907ArgfsTer11(p.E907Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218032
Start	12919412:12919412(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.377delA
AA Mutation	p.Asn126ThrfsTer2(p.N126Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218032
Start	12921072:12921072(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2037delT
AA Mutation	p.Phe679LeufsTer25(p.F679Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript