Mutation

Primary Site >> Stomach Cancer

Gene >> STAT4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191054526:191054526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215G>T
AA Mutation	p.Lys405Asn(p.K405N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191073130:191073130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>T
AA Mutation	p.His145Tyr(p.H145Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191146663:191146663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223A>G
AA Mutation	p.Lys75Glu(p.K75E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191036172:191036172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562A>G
AA Mutation	p.Lys521Arg(p.K521R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191033493:191033493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849A>T
AA Mutation	p.Ser617Cys(p.S617C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191076294:191076294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305C>T
AA Mutation	p.Ala102Val(p.A102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358470
Start	191033624:191033624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718A>G
AA Mutation	p.Tyr573Cys(p.Y573C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358470
Start	191032962:191032962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368928990
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358470
Start	191069730:191069730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199940585
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358470
Start	191033506:191033506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000358470
Start	191058026:191058026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Ter(p.R400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358470
Start	191033974:191033975(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1651dupT
AA Mutation	p.Trp551LeufsTer5(p.W551Lfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript