Mutation

Primary Site >> Stomach Cancer

Gene >> LGI3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148335:22148335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472A>G
AA Mutation	p.Gln491Arg(p.Q491R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148827:22148827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143158388
CDS Mutation	c.980G>A
AA Mutation	p.Arg327His(p.R327H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148903:22148903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757547343
CDS Mutation	c.904G>A
AA Mutation	p.Gly302Ser(p.G302S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148873:22148873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934A>G
AA Mutation	p.Thr312Ala(p.T312A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148509:22148509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113893603
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433His(p.R433H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148375:22148375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748894925
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22155398:22155398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272A>G
AA Mutation	p.Gln91Arg(p.Q91R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148684:22148684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138233100
CDS Mutation	c.1123C>T
AA Mutation	p.Arg375Cys(p.R375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148334:22148334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473G>T
AA Mutation	p.Gln491His(p.Q491H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306317
Start	22148683:22148683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124G>A
AA Mutation	p.Arg375His(p.R375H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22155421:22155421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142850097
CDS Mutation	c.249G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22154625:22154625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22148285:22148285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22155403:22155403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22148358:22148358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306317
Start	22151547:22151547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306317
Start	22156429:22156429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.114delC
AA Mutation	p.Cys39AlafsTer31(p.C39Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript