Mutation

Primary Site >> Stomach Cancer

Gene >> MYL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110911157:110911157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504559
CDS Mutation	c.421G>A
AA Mutation	p.Ala141Thr(p.A141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110919145:110919145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52T>G
AA Mutation	p.Phe18Val(p.F18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110914224:110914224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236T>G
AA Mutation	p.Phe79Cys(p.F79C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110919111:110919111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86T>G
AA Mutation	p.Phe29Cys(p.F29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110919160:110919160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894363
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228841
Start	110914249:110914249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211A>G
AA Mutation	p.Lys71Glu(p.K71E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228841
Start	110911143:110911143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766907447
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000228841
Start	110920526:110920526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000228841
Start	110919194:110919194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript