Mutation

Primary Site >> Stomach Cancer

Gene >> TNR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175403422:175403422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Glu232Lys(p.E232K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175403448:175403448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668G>A
AA Mutation	p.Ser223Asn(p.S223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175406344:175406344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175406591:175406591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124A>G
AA Mutation	p.Arg42Gly(p.R42G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175365963:175365963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2229T>A
AA Mutation	p.Asp743Glu(p.D743E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175403287:175403287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Ala277Thr(p.A277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175403508:175403508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608A>G
AA Mutation	p.Tyr203Cys(p.Y203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175386098:175386098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376305450
CDS Mutation	c.1711G>A
AA Mutation	p.Glu571Lys(p.E571K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175403296:175403296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820G>T
AA Mutation	p.Gly274Trp(p.G274W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175386140:175386140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669A>G
AA Mutation	p.Ser557Gly(p.S557G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175356369:175356369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3068C>T
AA Mutation	p.Ala1023Val(p.A1023V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263525
Start	175403614:175403614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>A
AA Mutation	p.Gln168Lys(p.Q168K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175386103:175386103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706G>A
AA Mutation	p.Arg569Gln(p.R569Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175365048:175365048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2549C>T
AA Mutation	p.Thr850Ile(p.T850I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175391324:175391324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771624358
CDS Mutation	c.1471G>A
AA Mutation	p.Ala491Thr(p.A491T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175367241:175367241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2020C>A
AA Mutation	p.Gln674Lys(p.Q674K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175330107:175330107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3760A>G
AA Mutation	p.Lys1254Glu(p.K1254E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263525
Start	175396544:175396544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78460048
CDS Mutation	c.1240C>T
AA Mutation	p.His414Tyr(p.H414Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263525
Start	175330076:175330076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3791C>T
AA Mutation	p.Ala1264Val(p.A1264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175356348:175356348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3089G>C
AA Mutation	p.Ser1030Thr(p.S1030T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175359727:175359727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2859G>T
AA Mutation	p.Met953Ile(p.M953I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175330091:175330091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3776G>A
AA Mutation	p.Ser1259Asn(p.S1259N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000263525
Start	175330217:175330217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773822782
CDS Mutation	c.3650G>T
AA Mutation	p.Arg1217Met(p.R1217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175365218:175365218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779560201
CDS Mutation	c.2379T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175403423:175403423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775081401
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175356389:175356389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3048C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175403585:175403585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175406292:175406292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175403582:175403582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550741218
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175386099:175386099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746969510
CDS Mutation	c.1710C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175337612:175337612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3450G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175324400:175324400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778628919
CDS Mutation	c.3913C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175355539:175355539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3213T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175356437:175356437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538886908
CDS Mutation	c.3000C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263525
Start	175362712:175362712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766628562
CDS Mutation	c.2805C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263525
Start	175365198:175365198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2399delC
AA Mutation	p.Pro800GlnfsTer18(p.P800Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000263525
Start	175363720:175363720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776846663
CDS Mutation	c.2695C>T
AA Mutation	p.Arg899Ter(p.R899*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263525
Start	175362672:175362673(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2844dupT
AA Mutation	p.Val949CysfsTer31(p.V949Cfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	39
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263525
Start	175396543:175396543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript