Mutation

Primary Site >> Stomach Cancer

Gene >> FOXO3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664257:108664257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424C>T
AA Mutation	p.Thr475Ile(p.T475I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108561291:108561291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83C>T
AA Mutation	p.Pro28Leu(p.P28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663582:108663582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749629630
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663767:108663767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Cys(p.R312C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663852:108663852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019A>G
AA Mutation	p.Asp340Gly(p.D340G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108561779:108561779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>A
AA Mutation	p.Val191Met(p.V191M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663581:108663581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Trp(p.R250W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664460:108664460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768999192
CDS Mutation	c.1627G>A
AA Mutation	p.Ala543Thr(p.A543T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108664461:108664461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628C>T
AA Mutation	p.Ala543Val(p.A543V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000343882
Start	108663497:108663497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Trp(p.R222W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664357:108664357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368666241
CDS Mutation	c.1524C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664039:108664039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343882
Start	108664096:108664096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343882
Start	108664046:108664046(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1217delG
AA Mutation	p.Gly406AspfsTer35(p.G406Dfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343882
Start	108663551:108663551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.723delG
AA Mutation	p.Lys242ArgfsTer117(p.K242Rfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript