Mutation

Primary Site >> Stomach Cancer

Gene >> MLIP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124808:54124808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>T
AA Mutation	p.Lys185Asn(p.K185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124731:54124731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769959762
CDS Mutation	c.478C>T
AA Mutation	p.Arg160Trp(p.R160W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124681:54124681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Ser143Asn(p.S143N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124635:54124635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>C
AA Mutation	p.Glu128Gln(p.E128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124567:54124567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Ile105Thr(p.I105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54149096:54149096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.653T>C
AA Mutation	p.Ile218Thr(p.I218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54230794:54230794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54169566:54169566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780054321
CDS Mutation	c.933C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54160784:54160784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274897
Start	54124707:54124707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.459delG
AA Mutation	p.Ile154LeufsTer11(p.I154Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000274897
Start	54257307:54257307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1318-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript