Mutation

Primary Site >> Stomach Cancer

Gene >> MTM1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150657899:150657899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587783755
CDS Mutation	c.1132G>A
AA Mutation	p.Gly378Arg(p.G378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150619074:150619074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>T
AA Mutation	p.Gly127Cys(p.G127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150645830:150645830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826A>G
AA Mutation	p.Ile276Val(p.I276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150645746:150645746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368335697
CDS Mutation	c.742G>A
AA Mutation	p.Gly248Ser(p.G248S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150641354:150641354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587783841
CDS Mutation	c.614C>T
AA Mutation	p.Pro205Leu(p.P205L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150641380:150641380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782761570
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Trp(p.R214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370396
Start	150649775:150649775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370396
Start	150614643:150614644(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.286_287insC
AA Mutation	p.Met96ThrfsTer7(p.M96Tfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000370396
Start	150649715:150649715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript