Mutation

Primary Site >> Stomach Cancer

Gene >> POU2F2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42093846:42093846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181G>T
AA Mutation	p.Ser394Ile(p.S394I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42117269:42117269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150784596
CDS Mutation	c.284C>T
AA Mutation	p.Thr95Met(p.T95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42099568:42099568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>T
AA Mutation	p.Ala154Ser(p.A154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42095574:42095574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Cys(p.R309C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42095578:42095578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42095307:42095307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42095337:42095337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192872020
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42099608:42099608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375042716
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42096214:42096214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000526816
Start	42092150:42092150(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1319delC
AA Mutation	p.Pro440ArgfsTer23(p.P440Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000526816
Start	42095391:42095392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1019_1025dupTGATCCG
AA Mutation	p.Val343AspfsTer161(p.V343Dfs*161)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript