Primary Site >> Stomach Cancer

Gene >> RRM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300738
Start 4127060:4127060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1496G>A
AA Mutation p.Arg499His(p.R499H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300738
Start 4135238:4135238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2158C>G
AA Mutation p.Leu720Val(p.L720V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300738
Start 4118445:4118445(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.776G>A
AA Mutation p.Gly259Asp(p.G259D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300738
Start 4138292:4138292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2288T>C
AA Mutation p.Val763Ala(p.V763A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300738
Start 4123199:4123199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1135C>T
AA Mutation p.Arg379Cys(p.R379C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000300738
Start 4129133:4129133(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1752C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000300738
Start 4112018:4112018(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.606G>A
Mutation Classification Silent
Feature Type Transcript