Mutation

Primary Site >> Stomach Cancer

Gene >> TEK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27173285:27173285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824A>C
AA Mutation	p.Lys275Thr(p.K275T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27206673:27206673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2456T>C
AA Mutation	p.Leu819Pro(p.L819P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27229176:27229176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3319C>T
AA Mutation	p.Leu1107Phe(p.L1107F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27217743:27217743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3047C>T
AA Mutation	p.Thr1016Ile(p.T1016I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27197495:27197495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1805T>C
AA Mutation	p.Leu602Pro(p.L602P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27212818:27212818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199701926
CDS Mutation	c.2798C>T
AA Mutation	p.Ala933Val(p.A933V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27206741:27206741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147231791
CDS Mutation	c.2524C>T
AA Mutation	p.Arg842Cys(p.R842C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27202839:27202839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929A>C
AA Mutation	p.Glu643Asp(p.E643D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27168531:27168531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401A>C
AA Mutation	p.Asp134Ala(p.D134A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27212862:27212862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2842G>A
AA Mutation	p.Val948Met(p.V948M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27190598:27190598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397G>T
AA Mutation	p.Ser466Ile(p.S466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27172730:27172730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>A
AA Mutation	p.Gly248Glu(p.G248E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27197503:27197503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1813T>A
AA Mutation	p.Leu605Ile(p.L605I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27228231:27228231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757379347
CDS Mutation	c.3226C>T
AA Mutation	p.Arg1076Trp(p.R1076W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000380036
Start	27203035:27203035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2125C>A
AA Mutation	p.Gln709Lys(p.Q709K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380036
Start	27185589:27185589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380036
Start	27203088:27203088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2178T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380036
Start	27204918:27204918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767259469
CDS Mutation	c.2217G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380036
Start	27185547:27185547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1250delC
AA Mutation	p.Pro417LeufsTer10(p.P417Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000380036
Start	27158097:27158097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Ter(p.R107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380036
Start	27190549:27190550(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1352dupC
AA Mutation	p.Asn452LysfsTer4(p.N452Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript