Primary Site >> Stomach Cancer

Gene >> ST6GALNAC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000156626
Start 76626314:76626314(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1390A>C
AA Mutation p.Met464Leu(p.M464L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000156626
Start 76629488:76629488(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355G>A
AA Mutation p.Ala119Thr(p.A119T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000156626
Start 76629319:76629319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138569950
CDS Mutation c.524C>T
AA Mutation p.Thr175Met(p.T175M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000156626
Start 76627081:76627081(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527809877
CDS Mutation c.1158C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000156626
Start 76627201:76627201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1038C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000156626
Start 76629133:76629133(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.710delC
AA Mutation p.Pro237LeufsTer15(p.P237Lfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000156626
Start 76626303:76626304(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1400dupA
AA Mutation p.Asn467LysfsTer41(p.N467Kfs*41)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript