Mutation

Primary Site >> Stomach Cancer

Gene >> MTUS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754090:17754090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718A>G
AA Mutation	p.Lys573Arg(p.K573R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754585:17754585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223C>T
AA Mutation	p.Ser408Leu(p.S408L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754531:17754531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277T>C
AA Mutation	p.Met426Thr(p.M426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17645963:17645963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148435996
CDS Mutation	c.3776C>T
AA Mutation	p.Ser1259Leu(p.S1259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754937:17754937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760128861
CDS Mutation	c.871G>A
AA Mutation	p.Ala291Thr(p.A291T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17753841:17753841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1967T>C
AA Mutation	p.Val656Ala(p.V656A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755557:17755557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251A>C
AA Mutation	p.Lys84Thr(p.K84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17743748:17743748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2143G>A
AA Mutation	p.Asp715Asn(p.D715N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754291:17754291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517A>T
AA Mutation	p.Asn506Ile(p.N506I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755086:17755086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>C
AA Mutation	p.Met241Thr(p.M241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17754220:17754220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588G>A
AA Mutation	p.Val530Ile(p.V530I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17743735:17743735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2156T>C
AA Mutation	p.Leu719Ser(p.L719S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262102
Start	17755638:17755638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170A>C
AA Mutation	p.Asp57Ala(p.D57A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17753924:17753924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1884G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17684502:17684502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2664C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17684442:17684442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17753933:17753933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201959113
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17653446:17653446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3267T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754551:17754551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754608:17754608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184944081
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262102
Start	17754320:17754320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754801:17754801(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1007delA
AA Mutation	p.Asn336IlefsTer2(p.N336Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754110:17754110(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1698delA
AA Mutation	p.Ala567GlnfsTer4(p.A567Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17655969:17655970(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3001dupA
AA Mutation	p.Thr1001AsnfsTer8(p.T1001Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754946:17754947(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.861_862insA
AA Mutation	p.Glu288ArgfsTer10(p.E288Rfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262102
Start	17754192:17754193(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1614_1615dupTG
AA Mutation	p.Ala539ValfsTer8(p.A539Vfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262102
Start	17647081:17647081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3502-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript