Mutation

Primary Site >> Stomach Cancer

Gene >> TLR9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223040:52223040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Cys(p.R426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221779:52221779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2537G>A
AA Mutation	p.Cys846Tyr(p.C846Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221372:52221372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142806370
CDS Mutation	c.2944C>T
AA Mutation	p.Arg982Trp(p.R982W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222400:52222400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771867596
CDS Mutation	c.1916G>A
AA Mutation	p.Arg639His(p.R639H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223202:52223202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>T
AA Mutation	p.His372Tyr(p.H372Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223549:52223549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202089021
CDS Mutation	c.767G>A
AA Mutation	p.Arg256His(p.R256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223625:52223625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Cys(p.R231C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223817:52223817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>A
AA Mutation	p.His167Asn(p.H167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221969:52221969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769171891
CDS Mutation	c.2347G>A
AA Mutation	p.Gly783Ser(p.G783S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223484:52223484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199797502
CDS Mutation	c.832G>A
AA Mutation	p.Asp278Asn(p.D278N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221351:52221351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747414072
CDS Mutation	c.2965C>T
AA Mutation	p.Arg989Cys(p.R989C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222116:52222116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200579725
CDS Mutation	c.2200G>A
AA Mutation	p.Ala734Thr(p.A734T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223576:52223576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749742285
CDS Mutation	c.740G>A
AA Mutation	p.Arg247His(p.R247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223630:52223630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686A>G
AA Mutation	p.Tyr229Cys(p.Y229C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52222042:52222042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144424164
CDS Mutation	c.2274C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221976:52221976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201639851
CDS Mutation	c.2340C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221532:52221532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2784T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223560:52223560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200139837
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52222525:52222525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52222519:52222519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143900156
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223934:52223934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760434000
CDS Mutation	c.382C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221367:52221367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2949G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52224016:52224016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201161379
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221241:52221241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3075C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223569:52223569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140856643
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360658
Start	52223738:52223738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.578delG
AA Mutation	p.Gly193ValfsTer51(p.G193Vfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360658
Start	52223001:52223001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1315delG
AA Mutation	p.Glu439ArgfsTer47(p.E439Rfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript