Primary Site >> Stomach Cancer

Gene >> MEF2D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000348159
Start 156468115:156468115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1432T>C
AA Mutation p.Tyr478His(p.Y478H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000348159
Start 156468784:156468784(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1243C>A
AA Mutation p.Leu415Ile(p.L415I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000348159
Start 156482594:156482594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.101A>C
AA Mutation p.Glu34Ala(p.E34A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000348159
Start 156482489:156482489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.206A>G
AA Mutation p.Tyr69Cys(p.Y69C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000348159
Start 156482448:156482448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.247G>A
AA Mutation p.Asp83Asn(p.D83N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000348159
Start 156477048:156477048(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.819C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000348159
Start 156468206:156468206(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1341T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000348159
Start 156479331:156479331(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.623delG
AA Mutation p.Gly208ValfsTer3(p.G208Vfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000348159
Start 156468244:156468244(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1303delC
AA Mutation p.His435ThrfsTer76(p.H435Tfs*76)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000348159
Start 156480896:156480896(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.334delC
AA Mutation p.Leu112CysfsTer58(p.L112Cfs*58)
Mutation Classification Frame_Shift_Del
Feature Type Transcript