Primary Site >> Stomach Cancer

Gene >> GALR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77250973:77250973(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756079511
CDS Mutation c.425G>A
AA Mutation p.Arg142His(p.R142H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77250961:77250961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413T>C
AA Mutation p.Val138Ala(p.V138A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77251132:77251132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.584G>A
AA Mutation p.Arg195His(p.R195H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77251059:77251059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.511G>A
AA Mutation p.Ala171Thr(p.A171T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77251002:77251002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.454G>A
AA Mutation p.Ala152Thr(p.A152T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000299727
Start 77250991:77250991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.443T>C
AA Mutation p.Val148Ala(p.V148A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000299727
Start 77251013:77251013(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.465C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000299727
Start 77250812:77250812(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.264C>T
Mutation Classification Silent
Feature Type Transcript