Mutation

Primary Site >> Stomach Cancer

Gene >> POU3F2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98834916:98834916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43A>G
AA Mutation	p.Ser15Gly(p.S15G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835715:98835715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842G>A
AA Mutation	p.Arg281Gln(p.R281Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835759:98835759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886G>A
AA Mutation	p.Gly296Ser(p.G296S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98834979:98834979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106G>A
AA Mutation	p.Glu36Lys(p.E36K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835598:98835598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.725C>T
AA Mutation	p.Pro242Leu(p.P242L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835806:98835806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933T>A
AA Mutation	p.Phe311Leu(p.F311L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98835647:98835647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98834936:98834936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763454533
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98836136:98836136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779168236
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328345
Start	98836152:98836152(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1284delG
AA Mutation	p.Ser429ValfsTer60(p.S429Vfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328345
Start	98835939:98835939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1070delA
AA Mutation	p.Lys357SerfsTer7(p.K357Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript