Mutation

Primary Site >> Stomach Cancer

Gene >> POU2F3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120305161:120305161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576G>T
AA Mutation	p.Glu192Asp(p.E192D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120309459:120309459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941T>C
AA Mutation	p.Ile314Thr(p.I314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120302326:120302326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367755083
CDS Mutation	c.402C>A
AA Mutation	p.Ser134Arg(p.S134R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120305741:120305741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764210023
CDS Mutation	c.725T>C
AA Mutation	p.Met242Thr(p.M242T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120298371:120298371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239T>A
AA Mutation	p.Leu80Gln(p.L80Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543440
Start	120309490:120309490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765069732
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543440
Start	120298273:120298273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139585451
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000543440
Start	120307585:120307585(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.877delC
AA Mutation	p.Arg293AlafsTer2(p.R293Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000543440
Start	120298392:120298392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000543440
Start	120298263:120298263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript