Primary Site >> Stomach Cancer

Gene >> RSRC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122508289:122508289(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964G>A
AA Mutation p.Ala322Thr(p.A322T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122517288:122517288(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753134403
CDS Mutation c.541C>T
AA Mutation p.Arg181Cys(p.R181C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122517296:122517296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.533C>T
AA Mutation p.Ser178Phe(p.S178F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122522166:122522166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.140C>T
AA Mutation p.Ser47Leu(p.S47L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122508233:122508233(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1020G>T
AA Mutation p.Gln340His(p.Q340H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000331738
Start 122517374:122517374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455G>A
AA Mutation p.Arg152Gln(p.R152Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000331738
Start 122505569:122505569(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1263T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000331738
Start 122521409:122521409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000331738
Start 122522234:122522234(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.72delA
AA Mutation p.Glu25SerfsTer78(p.E25Sfs*78)
Mutation Classification Frame_Shift_Del
Feature Type Transcript