Primary Site >> Stomach Cancer

Gene >> RBMXL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321792
Start 88983823:88983823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4G>C
AA Mutation p.Val2Leu(p.V2L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321792
Start 88983810:88983810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768543094
CDS Mutation c.17G>A
AA Mutation p.Arg6His(p.R6H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321792
Start 88983313:88983313(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514C>T
AA Mutation p.Arg172Cys(p.R172C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000321792
Start 88983644:88983644(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.183C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000321792
Start 88982924:88982924(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142293239
CDS Mutation c.903G>A
Mutation Classification Silent
Feature Type Transcript