Primary Site >> Stomach Cancer

Gene >> MYOD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000250003
Start 17719823:17719823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.41C>T
AA Mutation p.Thr14Met(p.T14M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000250003
Start 17720236:17720236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.454A>G
AA Mutation p.Asn152Asp(p.N152D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000250003
Start 17720275:17720275(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.493C>T
AA Mutation p.Arg165Cys(p.R165C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000250003
Start 17719858:17719858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76A>G
AA Mutation p.Thr26Ala(p.T26A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000250003
Start 17719895:17719895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.113C>T
AA Mutation p.Pro38Leu(p.P38L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000250003
Start 17719809:17719809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.27C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000250003
Start 17720388:17720388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.606G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000250003
Start 17720272:17720272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.490C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000250003
Start 17720916:17720916(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.650delC
AA Mutation p.Pro217ArgfsTer33(p.P217Rfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript