Mutation

Primary Site >> Stomach Cancer

Gene >> LIN9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226233439:226233439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Arg460Trp(p.R460W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226239060:226239060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752471823
CDS Mutation	c.1204C>T
AA Mutation	p.Arg402Trp(p.R402W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226267991:226267991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830T>G
AA Mutation	p.Leu277Arg(p.L277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226239062:226239062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202A>G
AA Mutation	p.Gln401Arg(p.Q401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328205
Start	226295927:226295927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>A
AA Mutation	p.Arg76Gln(p.R76Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328205
Start	226233110:226233110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371362225
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328205
Start	226233173:226233174(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1493_1494insTATGT
AA Mutation	p.Leu499MetfsTer3(p.L499Mfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000328205
Start	226287798:226287798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000328205
Start	226297813:226297875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.113-62_113delTTCATGGTATGAAATCCTTTGAACTAAGCCAAAATTCCATTAGTATTAACTATTTATTACAGA
Mutation Classification	Splice_Site
Feature Type	Transcript