Mutation

Primary Site >> Stomach Cancer

Gene >> LRRC3B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26709852:26709852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180A>T
AA Mutation	p.Arg60Ser(p.R60S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710096:26710096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424A>C
AA Mutation	p.Ile142Leu(p.I142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710043:26710043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>A
AA Mutation	p.Arg124Gln(p.R124Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710298:26710298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>T
AA Mutation	p.Thr209Ile(p.T209I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710276:26710276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604A>G
AA Mutation	p.Thr202Ala(p.T202A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26709874:26709874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202T>G
AA Mutation	p.Leu68Val(p.L68V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710154:26710154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749724681
CDS Mutation	c.482C>T
AA Mutation	p.Ala161Val(p.A161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710286:26710286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614C>T
AA Mutation	p.Ala205Val(p.A205V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396641
Start	26709961:26709961(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.293delA
AA Mutation	p.Asn98MetfsTer14(p.N98Mfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396641
Start	26710267:26710267(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.601delA
AA Mutation	p.Thr201LeufsTer17(p.T201Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript