Mutation

Primary Site >> Stomach Cancer

Gene >> APLP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879380:35879380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895G>A
AA Mutation	p.Arg632His(p.R632H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35878897:35878897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1658C>T
AA Mutation	p.Ala553Val(p.A553V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879389:35879389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904A>G
AA Mutation	p.Gln635Arg(p.Q635R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879415:35879415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1930T>C
AA Mutation	p.Tyr644His(p.Y644H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874636:35874636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189G>A
AA Mutation	p.Ala397Thr(p.A397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35879152:35879152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1792G>A
AA Mutation	p.Val598Ile(p.V598I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35872599:35872599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778308918
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Cys(p.R323C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35874543:35874543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096T>C
AA Mutation	p.Ser366Pro(p.S366P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000221891
Start	35878918:35878918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1679C>A
AA Mutation	p.Pro560His(p.P560H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35879136:35879136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376643850
CDS Mutation	c.1776C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35872547:35872547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221891
Start	35878606:35878606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221891
Start	35871880:35871880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.698delC
AA Mutation	p.Pro233ArgfsTer5(p.P233Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221891
Start	35871704:35871705(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.635dupC
AA Mutation	p.Pro213SerfsTer13(p.P213Sfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript