Mutation

Primary Site >> Stomach Cancer

Gene >> LGMN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92709736:92709736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956T>C
AA Mutation	p.Leu319Pro(p.L319P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92714428:92714428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428T>G
AA Mutation	p.Ile143Ser(p.I143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92709851:92709851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841A>C
AA Mutation	p.Met281Leu(p.M281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92709824:92709824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>A
AA Mutation	p.Ala290Thr(p.A290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334869
Start	92709734:92709734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777103735
CDS Mutation	c.958A>G
AA Mutation	p.Met320Val(p.M320V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92711921:92711921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334869
Start	92709813:92709813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000334869
Start	92704642:92704642(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1257delC
AA Mutation	p.His419GlnfsTer3(p.H419Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334869
Start	92709805:92709806(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.886dupC
AA Mutation	p.Leu296ProfsTer8(p.L296Pfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript