Mutation

Primary Site >> Stomach Cancer

Gene >> MTUS2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29026890:29026890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2222A>C
AA Mutation	p.Lys741Thr(p.K741T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29033964:29033964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2315C>T
AA Mutation	p.Ser772Leu(p.S772L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29025423:29025423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373199820
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29026832:29026832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552392007
CDS Mutation	c.2164G>A
AA Mutation	p.Gly722Arg(p.G722R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29359339:29359339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764265852
CDS Mutation	c.3013C>T
AA Mutation	p.Arg1005Trp(p.R1005W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29026892:29026892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2224T>A
AA Mutation	p.Phe742Ile(p.F742I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29025071:29025071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201510503
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Trp(p.R135W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29503144:29503144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151024742
CDS Mutation	c.4078G>A
AA Mutation	p.Val1360Ile(p.V1360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29281862:29281862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377003171
CDS Mutation	c.2833G>A
AA Mutation	p.Ala945Thr(p.A945T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29033943:29033943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200475426
CDS Mutation	c.2294T>C
AA Mutation	p.Val765Ala(p.V765A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29034096:29034096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2447C>T
AA Mutation	p.Ala816Val(p.A816V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29281839:29281839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2810C>T
AA Mutation	p.Ala937Val(p.A937V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29026140:29026140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576095515
CDS Mutation	c.1472C>T
AA Mutation	p.Thr491Met(p.T491M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29024802:29024802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548916506
CDS Mutation	c.134C>T
AA Mutation	p.Thr45Met(p.T45M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29281821:29281821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2792G>A
AA Mutation	p.Arg931His(p.R931H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29492651:29492651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3541A>G
AA Mutation	p.Met1181Val(p.M1181V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29497298:29497298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775222983
CDS Mutation	c.3670G>A
AA Mutation	p.Glu1224Lys(p.E1224K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29026739:29026739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747494603
CDS Mutation	c.2071G>A
AA Mutation	p.Glu691Lys(p.E691K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29498520:29498520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3811C>T
AA Mutation	p.Leu1271Phe(p.L1271F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000612955
Start	29025712:29025712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044G>T
AA Mutation	p.Glu348Asp(p.E348D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29503131:29503131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776955739
CDS Mutation	c.4065G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29487914:29487914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760952656
CDS Mutation	c.3444C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29026525:29026525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29026528:29026528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1860C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29024854:29024854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612955
Start	29026531:29026531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748912007
CDS Mutation	c.1863G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000612955
Start	29026415:29026415(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1751delC
AA Mutation	p.Pro584LeufsTer8(p.P584Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000612955
Start	29033938:29033938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2289T>G
AA Mutation	p.Tyr763Ter(p.Y763*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000612955
Start	29025483:29025484(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.820dupG
AA Mutation	p.Ala274GlyfsTer9(p.A274Gfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript