Mutation

Primary Site >> Stomach Cancer

Gene >> BRINP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119208782:119208782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746081030
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361His(p.R361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119208765:119208765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099A>C
AA Mutation	p.Ser367Arg(p.S367R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167290:119167290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2080C>T
AA Mutation	p.Leu694Phe(p.L694F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119208779:119208779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085A>G
AA Mutation	p.Lys362Arg(p.K362R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167397:119167397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1973T>A
AA Mutation	p.Phe658Tyr(p.F658Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167385:119167385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1985T>A
AA Mutation	p.Leu662Gln(p.L662Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167529:119167529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841C>T
AA Mutation	p.Thr614Met(p.T614M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167512:119167512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745883942
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Cys(p.R620C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119242102:119242102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151157979
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119208897:119208897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967C>A
AA Mutation	p.Leu323Met(p.L323M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119249104:119249104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Asp89Asn(p.D89N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119168006:119168006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364A>C
AA Mutation	p.Lys455Thr(p.K455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119208854:119208854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010A>G
AA Mutation	p.Asp337Gly(p.D337G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167884:119167884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>A
AA Mutation	p.Asp496Asn(p.D496N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167761:119167761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762203463
CDS Mutation	c.1609T>G
AA Mutation	p.Phe537Val(p.F537V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119214009:119214009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832T>C
AA Mutation	p.Cys278Arg(p.C278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167637:119167637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1733C>T
AA Mutation	p.Pro578Leu(p.P578L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167878:119167878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Cys(p.R498C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119249043:119249043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326G>T
AA Mutation	p.Gly109Val(p.G109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119313343:119313343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13T>G
AA Mutation	p.Phe5Val(p.F5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000265922
Start	119167716:119167716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654C>T
AA Mutation	p.Arg552Cys(p.R552C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119167534:119167534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119167300:119167300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141113114
CDS Mutation	c.2070G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119238695:119238695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373900703
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119167606:119167606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1764G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119167408:119167408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750068438
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119249009:119249009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119249138:119249138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119167129:119167129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119249042:119249042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265922
Start	119249093:119249093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript