Mutation

Primary Site >> Stomach Cancer

Gene >> MTSS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553288:124553288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972A>G
AA Mutation	p.Thr658Ala(p.T658A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553462:124553462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Cys(p.R600C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553432:124553432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828C>A
AA Mutation	p.Pro610Thr(p.P610T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553191:124553191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069T>A
AA Mutation	p.Ile690Asn(p.I690N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553260:124553260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000G>A
AA Mutation	p.Gly667Asp(p.G667D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553128:124553128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2132A>G
AA Mutation	p.Gln711Arg(p.Q711R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000518547
Start	124553146:124553146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776642168
CDS Mutation	c.2114C>T
AA Mutation	p.Ala705Val(p.A705V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518547
Start	124591204:124591204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518547
Start	124585121:124585121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747793159
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518547
Start	124553277:124553277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1983C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518547
Start	124553262:124553262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762286207
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000518547
Start	124585088:124585088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.459delA
AA Mutation	p.Arg155GlufsTer34(p.R155Efs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518547
Start	124556317:124556317(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1319delG
AA Mutation	p.Gly440GlufsTer22(p.G440Efs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518547
Start	124553336:124553336(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1924delG
AA Mutation	p.Glu642SerfsTer79(p.E642Sfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript