Primary Site >> Stomach Cancer

Gene >> CTRL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000574481
Start 67930500:67930500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.407G>T
AA Mutation p.Arg136Leu(p.R136L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000574481
Start 67930500:67930500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746032624
CDS Mutation c.407G>A
AA Mutation p.Arg136His(p.R136H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000574481
Start 67930751:67930751(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.293C>A
AA Mutation p.Pro98His(p.P98H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000574481
Start 67931146:67931146(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146079104
CDS Mutation c.108C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000574481
Start 67930296:67930296(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.522G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000574481
Start 67930735:67930735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309C>T
Mutation Classification Silent
Feature Type Transcript