Mutation

Primary Site >> Stomach Cancer

Gene >> APBA1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69431352:69431352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2489C>T
AA Mutation	p.Ala830Val(p.A830V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516681:69516681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69452241:69452241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849A>G
AA Mutation	p.Arg617Gly(p.R617G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69467921:69467921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516363:69516363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>T
AA Mutation	p.Ser283Leu(p.S283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69431386:69431386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2455A>G
AA Mutation	p.Thr819Ala(p.T819A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516778:69516778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516607:69516607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>T
AA Mutation	p.Gly202Trp(p.G202W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69452205:69452205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1885A>G
AA Mutation	p.Lys629Glu(p.K629E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69432654:69432654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2324G>A
AA Mutation	p.Gly775Glu(p.G775E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516577:69516577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763263675
CDS Mutation	c.634G>A
AA Mutation	p.Gly212Ser(p.G212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516201:69516201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750949378
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337Gln(p.R337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69431348:69431348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2493G>T
AA Mutation	p.Gln831His(p.Q831H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265381
Start	69516723:69516723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488C>T
AA Mutation	p.Ala163Val(p.A163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69516086:69516086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774728152
CDS Mutation	c.1125A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69452281:69452281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1809C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69467919:69467919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141287424
CDS Mutation	c.1386C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69516473:69516473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69516833:69516833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69432623:69432623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2355G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265381
Start	69456313:69456313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186990223
CDS Mutation	c.1722G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265381
Start	69516300:69516300(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.911delC
AA Mutation	p.Pro304LeufsTer57(p.P304Lfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265381
Start	69452128:69452129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1961_1962delGT
AA Mutation	p.Cys654Ter(p.C654*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265381
Start	69441116:69441116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2182-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript