Primary Site >> Stomach Cancer

Gene >> CSRP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311083
Start 76866155:76866155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.106C>G
AA Mutation p.Leu36Val(p.L36V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311083
Start 76859618:76859618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434G>A
AA Mutation p.Arg145Gln(p.R145Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000311083
Start 76860386:76860386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000311083
Start 76859006:76859006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.528G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000311083
Start 76860282:76860282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.411+2T>C
Mutation Classification Splice_Site
Feature Type Transcript