Primary Site >> Stomach Cancer

Gene >> CMTR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71285125:71285125(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766157732
CDS Mutation c.796C>G
AA Mutation p.Leu266Val(p.L266V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71284711:71284711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1210T>G
AA Mutation p.Phe404Val(p.F404V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71284783:71284783(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769589947
CDS Mutation c.1138C>T
AA Mutation p.Arg380Cys(p.R380C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71284759:71284759(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1162G>T
AA Mutation p.Ala388Ser(p.A388S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71284164:71284164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1757C>T
AA Mutation p.Ser586Leu(p.S586L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71283724:71283724(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2197G>A
AA Mutation p.Gly733Arg(p.G733R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000338099
Start 71284229:71284229(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1692G>C
AA Mutation p.Glu564Asp(p.E564D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000338099
Start 71284094:71284094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1827T>C
Mutation Classification Silent
Feature Type Transcript