Mutation

Primary Site >> Stomach Cancer

Gene >> INF2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104711695:104711695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485G>A
AA Mutation	p.Ala829Thr(p.A829T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104713543:104713543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2977C>T
AA Mutation	p.Arg993Cys(p.R993C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104703412:104703412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625G>A
AA Mutation	p.Glu209Lys(p.E209K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104707934:104707934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753323267
CDS Mutation	c.1667G>A
AA Mutation	p.Arg556Gln(p.R556Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392634
Start	104712498:104712498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372129830
CDS Mutation	c.2555G>A
AA Mutation	p.Arg852Gln(p.R852Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104707980:104707980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1713G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392634
Start	104703351:104703351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746732992
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104707848:104707848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1587delC
AA Mutation	p.Val530TrpfsTer28(p.V530Wfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392634
Start	104708559:104708559(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1864delC
AA Mutation	p.Arg622GlyfsTer18(p.R622Gfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript