Mutation

Primary Site >> Stomach Cancer

Gene >> IGF2BP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23418792:23418792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269C>A
AA Mutation	p.Pro90His(p.P90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23312450:23312450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652G>T
AA Mutation	p.Arg551Ile(p.R551I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23345976:23345976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905T>A
AA Mutation	p.Ile302Asn(p.I302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23319239:23319239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1219A>G
AA Mutation	p.Thr407Ala(p.T407A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23469973:23469973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23468499:23468499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23312398:23312398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23347689:23347689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756431557
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258729
Start	23345977:23345977(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.904delA
AA Mutation	p.Ile302LeufsTer17(p.I302Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258729
Start	23345976:23345977(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.904dupA
AA Mutation	p.Ile302AsnfsTer2(p.I302Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000258729
Start	23319136:23319136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1320+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000258729
Start	23319256:23319256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript