Mutation

Primary Site >> Stomach Cancer

Gene >> APBA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29106643:29106643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757921952
CDS Mutation	c.1741G>A
AA Mutation	p.Val581Met(p.V581M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29053894:29053894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755550991
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Trp(p.R4W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29113951:29113951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753314225
CDS Mutation	c.2113G>A
AA Mutation	p.Gly705Arg(p.G705R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29076079:29076079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057A>G
AA Mutation	p.Ser353Gly(p.S353G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29093089:29093089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084G>A
AA Mutation	p.Glu362Lys(p.E362K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29113933:29113933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755413618
CDS Mutation	c.2095C>T
AA Mutation	p.Arg699Cys(p.R699C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29105410:29105410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746149119
CDS Mutation	c.1556C>T
AA Mutation	p.Ala519Val(p.A519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29113942:29113942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2104G>A
AA Mutation	p.Glu702Lys(p.E702K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29113934:29113934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096G>A
AA Mutation	p.Arg699His(p.R699H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29053975:29053975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91A>G
AA Mutation	p.Ser31Gly(p.S31G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29101659:29101659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399G>T
AA Mutation	p.Val467Leu(p.V467L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29106760:29106760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1858T>A
AA Mutation	p.Ser620Thr(p.S620T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29054720:29054720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>T
AA Mutation	p.Ala279Val(p.A279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29054786:29054786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902A>G
AA Mutation	p.Lys301Arg(p.K301R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29054206:29054206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771125386
CDS Mutation	c.322G>A
AA Mutation	p.Asp108Asn(p.D108N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000558259
Start	29105470:29105470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616G>A
AA Mutation	p.Ser539Asn(p.S539N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29054235:29054235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772215906
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29053956:29053956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29054052:29054052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367887200
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29117082:29117082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779082827
CDS Mutation	c.2199C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29093149:29093149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558259
Start	29054427:29054427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000558259
Start	29114017:29114017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2178+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript