Mutation

Primary Site >> Stomach Cancer

Gene >> PBXIP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154953684:154953684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38T>G
AA Mutation	p.Leu13Arg(p.L13R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946776:154946776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898A>T
AA Mutation	p.Met300Leu(p.M300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946778:154946778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896T>C
AA Mutation	p.Leu299Pro(p.L299P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946753:154946753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921G>T
AA Mutation	p.Glu307Asp(p.E307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154951900:154951900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73G>T
AA Mutation	p.Gly25Cys(p.G25C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946142:154946142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511Lys(p.R511K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154948362:154948362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414G>C
AA Mutation	p.Trp138Cys(p.W138C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154945609:154945609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065T>G
AA Mutation	p.Phe689Val(p.F689V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154948283:154948283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372020762
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946632:154946632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766767263
CDS Mutation	c.1042G>A
AA Mutation	p.Gly348Ser(p.G348S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368463
Start	154946786:154946786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368463
Start	154953713:154953713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368463
Start	154951840:154951841(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.132_133insA
AA Mutation	p.Ser45IlefsTer22(p.S45Ifs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript