Primary Site >> Stomach Cancer

Gene >> FUT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750647:48750647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.635G>A
AA Mutation p.Arg212His(p.R212H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48751020:48751020(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.262C>G
AA Mutation p.Arg88Gly(p.R88G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750665:48750665(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750207214
CDS Mutation c.617G>A
AA Mutation p.Arg206His(p.R206H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750497:48750497(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.785G>A
AA Mutation p.Ser262Asn(p.S262N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750653:48750653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.629G>A
AA Mutation p.Arg210His(p.R210H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48751198:48751198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.84T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48751066:48751066(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.216G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48751099:48751099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750862:48750862(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.420G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750649:48750649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.633G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750229:48750229(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750580:48750580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.702T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750508:48750508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.774C>T
Mutation Classification Silent
Feature Type Transcript