Mutation

Primary Site >> Stomach Cancer

Gene >> TNIK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171194551:171194551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171079563:171079563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3403T>C
AA Mutation	p.Trp1135Arg(p.W1135R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171369679:171369679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64G>A
AA Mutation	p.Ala22Thr(p.A22T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171211216:171211216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206A>T
AA Mutation	p.Glu69Val(p.E69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171228175:171228175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170A>T
AA Mutation	p.Asp57Val(p.D57V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171079574:171079574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3392A>G
AA Mutation	p.Lys1131Arg(p.K1131R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171084242:171084242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3082A>G
AA Mutation	p.Thr1028Ala(p.T1028A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171066272:171066272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3914G>A
AA Mutation	p.Arg1305Gln(p.R1305Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171194599:171194599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Asp115Asn(p.D115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171101520:171101520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2520G>T
AA Mutation	p.Glu840Asp(p.E840D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171188739:171188739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602C>T
AA Mutation	p.Ala201Val(p.A201V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171066212:171066212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3974A>C
AA Mutation	p.Lys1325Thr(p.K1325T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000436636
Start	171087383:171087383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369860165
CDS Mutation	c.2845C>T
AA Mutation	p.Arg949Cys(p.R949C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436636
Start	171087459:171087459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2769T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436636
Start	171139488:171139488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436636
Start	171167261:171167261(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.783delA
AA Mutation	p.Lys261AsnfsTer11(p.K261Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000436636
Start	171063946:171063946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4018C>T
AA Mutation	p.Arg1340Ter(p.R1340*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000436636
Start	171139544:171139544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345C>T
AA Mutation	p.Arg449Ter(p.R449*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000436636
Start	171125938:171125938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987C>T
AA Mutation	p.Arg663Ter(p.R663*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000436636
Start	171079625:171079627(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3339_3341delCTA
AA Mutation	p.Tyr1114del(p.Y1114del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript