Primary Site >> Stomach Cancer

Gene >> SLC29A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371708
Start 44232414:44232414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1045G>T
AA Mutation p.Ala349Ser(p.A349S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371708
Start 44230661:44230661(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200092000
CDS Mutation c.683G>A
AA Mutation p.Arg228His(p.R228H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371708
Start 44232924:44232924(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1177G>A
AA Mutation p.Asp393Asn(p.D393N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000371708
Start 44229985:44229985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.393G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000371708
Start 44229462:44229462(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756909033
CDS Mutation c.102G>A
Mutation Classification Silent
Feature Type Transcript