Mutation

Primary Site >> Stomach Cancer

Gene >> TYK2

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264818
Start	10366417:10366417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>T
AA Mutation	p.Ser210Ile(p.S210I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10350961:10350961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3437A>G
AA Mutation	p.His1146Arg(p.H1146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10356594:10356594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770219068
CDS Mutation	c.2591G>A
AA Mutation	p.Arg864His(p.R864H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10352953:10352953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3173G>A
AA Mutation	p.Arg1058His(p.R1058H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10364933:10364933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127A>G
AA Mutation	p.Tyr376Cys(p.Y376C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10365804:10365804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724C>A
AA Mutation	p.Leu242Met(p.L242M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10364937:10364937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773725258
CDS Mutation	c.1123G>A
AA Mutation	p.Ala375Thr(p.A375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10354564:10354564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2663A>G
AA Mutation	p.Asp888Gly(p.D888G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10352940:10352940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767739960
CDS Mutation	c.3186C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10354569:10354569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761205319
CDS Mutation	c.2658G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10378365:10378365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543965548
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10361848:10361848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759253619
CDS Mutation	c.1881C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10368324:10368324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10353078:10353078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3048G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10365658:10365658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264818
Start	10357899:10357899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2331delC
AA Mutation	p.Trp778GlyfsTer14(p.W778Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264818
Start	10365598:10365598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.930delG
AA Mutation	p.Pro312GlnfsTer7(p.P312Qfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264818
Start	10361850:10361850(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1879delC
AA Mutation	p.Leu627SerfsTer36(p.L627Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript