Mutation

Primary Site >> Stomach Cancer

Gene >> TCHH

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109333:152109333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3884A>G
AA Mutation	p.Glu1295Gly(p.E1295G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110019:152110019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3198G>T
AA Mutation	p.Glu1066Asp(p.E1066D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108296:152108296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4921C>T
AA Mutation	p.Arg1641Cys(p.R1641C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109085:152109085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369543263
CDS Mutation	c.4132G>A
AA Mutation	p.Glu1378Lys(p.E1378K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107557:152107557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5660G>A
AA Mutation	p.Arg1887His(p.R1887H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109466:152109466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182639950
CDS Mutation	c.3751C>T
AA Mutation	p.Arg1251Trp(p.R1251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108967:152108967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370960477
CDS Mutation	c.4250G>A
AA Mutation	p.Arg1417His(p.R1417H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107576:152107576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760165446
CDS Mutation	c.5641C>T
AA Mutation	p.Arg1881Trp(p.R1881W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109228:152109228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3989G>A
AA Mutation	p.Arg1330His(p.R1330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108488:152108488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4729C>T
AA Mutation	p.Arg1577Cys(p.R1577C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108751:152108751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4466A>G
AA Mutation	p.Glu1489Gly(p.E1489G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109141:152109141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4076A>G
AA Mutation	p.Asp1359Gly(p.D1359G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110066:152110066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779106201
CDS Mutation	c.3151C>T
AA Mutation	p.Arg1051Trp(p.R1051W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111329:152111329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1888C>T
AA Mutation	p.Arg630Cys(p.R630C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112899:152112899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>T
AA Mutation	p.Lys106Asn(p.K106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152113030:152113030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187C>T
AA Mutation	p.Leu63Phe(p.L63F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109291:152109291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3926G>T
AA Mutation	p.Arg1309Met(p.R1309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110701:152110701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2516A>G
AA Mutation	p.Gln839Arg(p.Q839R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107920:152107920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5297G>A
AA Mutation	p.Arg1766His(p.R1766H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108256:152108256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775186687
CDS Mutation	c.4961G>A
AA Mutation	p.Arg1654His(p.R1654H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109910:152109910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576125673
CDS Mutation	c.3307C>T
AA Mutation	p.Arg1103Cys(p.R1103C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108033:152108033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5184G>T
AA Mutation	p.Glu1728Asp(p.E1728D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110875:152110875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2342G>A
AA Mutation	p.Arg781His(p.R781H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112995:152112995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>A
AA Mutation	p.Phe74Leu(p.F74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112943:152112943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274G>A
AA Mutation	p.Ala92Thr(p.A92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108233:152108233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528288947
CDS Mutation	c.4984C>T
AA Mutation	p.Arg1662Cys(p.R1662C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112235:152112235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Cys(p.R328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110938:152110938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2279A>G
AA Mutation	p.Glu760Gly(p.E760G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108221:152108221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757699851
CDS Mutation	c.4996G>A
AA Mutation	p.Asp1666Asn(p.D1666N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108367:152108367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370364413
CDS Mutation	c.4850G>A
AA Mutation	p.Arg1617His(p.R1617H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109881:152109881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3336G>T
AA Mutation	p.Glu1112Asp(p.E1112D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107705:152107705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5512C>T
AA Mutation	p.Arg1838Trp(p.R1838W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110445:152110445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2772A>C
AA Mutation	p.Gln924His(p.Q924H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108115:152108115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5102G>A
AA Mutation	p.Arg1701His(p.R1701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108896:152108896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4321C>T
AA Mutation	p.Arg1441Cys(p.R1441C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110179:152110179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3038G>A
AA Mutation	p.Arg1013His(p.R1013H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111656:152111656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Cys(p.R521C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111219:152111219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1998G>T
AA Mutation	p.Glu666Asp(p.E666D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107897:152107897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776770509
CDS Mutation	c.5320C>T
AA Mutation	p.Arg1774Cys(p.R1774C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108719:152108719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4498G>A
AA Mutation	p.Asp1500Asn(p.D1500N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112798:152112798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770478540
CDS Mutation	c.419A>C
AA Mutation	p.Lys140Thr(p.K140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109705:152109705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3512G>A
AA Mutation	p.Arg1171His(p.R1171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112471:152112471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746G>A
AA Mutation	p.Arg249His(p.R249H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152113015:152113015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152108966:152108966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4251C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152114024:152114024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152108783:152108783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4434G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152111270:152111270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565627723
CDS Mutation	c.1947C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152111518:152111518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1699C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152108426:152108426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4791C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152109754:152109754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3463A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152109017:152109017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4200C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368804
Start	152108198:152108198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5019delA
AA Mutation	p.Glu1673AspfsTer78(p.E1673Dfs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368804
Start	152110293:152110293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2924delG
AA Mutation	p.Gly975GlufsTer30(p.G975Efs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	55
Mutation Consequence	stop_gained
Transcription ID	ENST00000368804
Start	152109958:152109958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3259C>T
AA Mutation	p.Gln1087Ter(p.Q1087*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368804
Start	152110147:152110148(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3069dupA
AA Mutation	p.Asp1024ArgfsTer194(p.D1024Rfs*194)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript