Mutation

Primary Site >> Stomach Cancer

Gene >> MUSK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110775930:110775930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327G>A
AA Mutation	p.Asp443Asn(p.D443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110787797:110787797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886T>C
AA Mutation	p.Leu629Pro(p.L629P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110767870:110767870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971T>A
AA Mutation	p.Val324Glu(p.V324E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800665:110800665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199507468
CDS Mutation	c.2287G>A
AA Mutation	p.Ala763Thr(p.A763T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110775937:110775937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334C>T
AA Mutation	p.Thr445Met(p.T445M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110687137:110687137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227G>A
AA Mutation	p.Ser76Asn(p.S76N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800452:110800452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2074C>G
AA Mutation	p.Pro692Ala(p.P692A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800381:110800381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777865246
CDS Mutation	c.2003G>A
AA Mutation	p.Arg668His(p.R668H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800442:110800442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064G>T
AA Mutation	p.Gln688His(p.Q688H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110787793:110787793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776795823
CDS Mutation	c.1882G>A
AA Mutation	p.Ala628Thr(p.A628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110734269:110734269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188464904
CDS Mutation	c.647G>A
AA Mutation	p.Arg216Gln(p.R216Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110747737:110747737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Ala284Ser(p.A284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800884:110800884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769657813
CDS Mutation	c.2506C>T
AA Mutation	p.Arg836Cys(p.R836C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110800864:110800864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2486T>A
AA Mutation	p.Val829Glu(p.V829E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110767851:110767851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369023786
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374448
Start	110785586:110785586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1646A>G
AA Mutation	p.His549Arg(p.H549R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374448
Start	110785614:110785614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541645382
CDS Mutation	c.1674G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374448
Start	110767844:110767844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374448
Start	110800820:110800820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779578271
CDS Mutation	c.2442C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374448
Start	110682753:110682753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374448
Start	110800699:110800699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2326delT
AA Mutation	p.Tyr776IlefsTer92(p.Y776Ifs*92)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374448
Start	110697413:110697414(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.581dupA
AA Mutation	p.Asn194LysfsTer16(p.N194Kfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript