Mutation

Primary Site >> Stomach Cancer

Gene >> TPR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186359851:186359851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200390468
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446His(p.R446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186359866:186359866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441His(p.R441H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186334415:186334415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764775414
CDS Mutation	c.5092C>T
AA Mutation	p.Arg1698Cys(p.R1698C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186341331:186341331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3809A>C
AA Mutation	p.Asn1270Thr(p.N1270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186327521:186327521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5828T>C
AA Mutation	p.Val1943Ala(p.V1943A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367478
Start	186356447:186356447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727T>C
AA Mutation	p.Ile576Thr(p.I576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186344526:186344526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3266A>G
AA Mutation	p.His1089Arg(p.H1089R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186352099:186352099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2346A>C
AA Mutation	p.Glu782Asp(p.E782D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186355762:186355762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1895G>A
AA Mutation	p.Ser632Asn(p.S632N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186359867:186359867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Cys(p.R441C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186314659:186314659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7006G>A
AA Mutation	p.Val2336Ile(p.V2336I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186318583:186318583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6685A>G
AA Mutation	p.Thr2229Ala(p.T2229A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186322390:186322390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6389A>C
AA Mutation	p.Glu2130Ala(p.E2130A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186333155:186333155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5422C>T
AA Mutation	p.Arg1808Trp(p.R1808W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186346210:186346210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3021G>T
AA Mutation	p.Lys1007Asn(p.K1007N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186357454:186357454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667C>T
AA Mutation	p.Ala556Val(p.A556V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186355458:186355458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781372334
CDS Mutation	c.2123G>A
AA Mutation	p.Arg708Gln(p.R708Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186332229:186332229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5570A>C
AA Mutation	p.Lys1857Thr(p.K1857T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186350243:186350243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2756C>G
AA Mutation	p.Ser919Cys(p.S919C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186331535:186331535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5651A>G
AA Mutation	p.Gln1884Arg(p.Q1884R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367478
Start	186357397:186357397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724A>C
AA Mutation	p.Lys575Thr(p.K575T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186370977:186370977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>T
AA Mutation	p.Ala108Val(p.A108V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000367478
Start	186343408:186343408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3668G>A
AA Mutation	p.Arg1223His(p.R1223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186360336:186360336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377515093
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186333336:186333336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575105371
CDS Mutation	c.5241C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186356380:186356380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186335452:186335452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4797T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186327565:186327565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5784G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186332270:186332270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5529A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186370976:186370976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186331519:186331519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5667T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186336644:186336644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4557G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367478
Start	186333318:186333318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5259T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367478
Start	186322398:186322398(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6381delT
AA Mutation	p.Phe2127LeufsTer65(p.F2127Lfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000367478
Start	186341368:186341368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3772C>T
AA Mutation	p.Gln1258Ter(p.Q1258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript