Mutation

Primary Site >> Stomach Cancer

Gene >> BRINP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098943:190098943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776492382
CDS Mutation	c.1376G>A
AA Mutation	p.Arg459His(p.R459H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190264951:190264951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775664699
CDS Mutation	c.532C>T
AA Mutation	p.His178Tyr(p.H178Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190226117:190226117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926C>A
AA Mutation	p.Thr309Asn(p.T309N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190281715:190281715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272T>C
AA Mutation	p.Val91Ala(p.V91A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098368:190098368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1951T>G
AA Mutation	p.Phe651Val(p.F651V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190226270:190226270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773C>A
AA Mutation	p.Ala258Glu(p.A258E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098502:190098502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817A>G
AA Mutation	p.Gln606Arg(p.Q606R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098163:190098163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760188757
CDS Mutation	c.2156G>A
AA Mutation	p.Arg719His(p.R719H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190226102:190226102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>G
AA Mutation	p.Asn314Ser(p.N314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190264869:190264869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614T>G
AA Mutation	p.Ile205Arg(p.I205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098792:190098792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527A>C
AA Mutation	p.Glu509Asp(p.E509D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098686:190098686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1633A>C
AA Mutation	p.Ser545Arg(p.S545R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098325:190098325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1994A>G
AA Mutation	p.Asn665Ser(p.N665S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367462
Start	190454655:190454655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236G>A
AA Mutation	p.Arg79Lys(p.R79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367462
Start	190160668:190160668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184G>T
AA Mutation	p.Arg395Ile(p.R395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098424:190098424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751255099
CDS Mutation	c.1895G>A
AA Mutation	p.Arg632His(p.R632H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098690:190098690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1629G>C
AA Mutation	p.Lys543Asn(p.K543N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098730:190098730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530His(p.R530H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098425:190098425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1894C>T
AA Mutation	p.Arg632Cys(p.R632C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098037:190098037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761166562
CDS Mutation	c.2282C>T
AA Mutation	p.Thr761Met(p.T761M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098418:190098418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1901A>C
AA Mutation	p.Lys634Thr(p.K634T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098483:190098483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836A>C
AA Mutation	p.Leu612Phe(p.L612F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000367462
Start	190098514:190098514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805A>G
AA Mutation	p.Asp602Gly(p.D602G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098939:190098939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098510:190098510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1809A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098966:190098966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1353A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190099080:190099080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098471:190098471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1848C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098705:190098705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1614G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190226116:190226116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190160822:190160822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098474:190098474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1845G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098075:190098075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562180986
CDS Mutation	c.2244G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367462
Start	190098834:190098834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768599124
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367462
Start	190098453:190098453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1866delT
AA Mutation	p.Phe622LeufsTer8(p.F622Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000367462
Start	190098732:190098732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587G>A
AA Mutation	p.Trp529Ter(p.W529*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript