Primary Site >> Stomach Cancer

Gene >> RIPK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000220751
Start 89769865:89769865(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.577A>C
AA Mutation p.Met193Leu(p.M193L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000220751
Start 89758150:89758150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.90C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000220751
Start 89772743:89772743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.768A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000220751
Start 89769855:89769855(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.567A>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000220751
Start 89758168:89758168(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.108C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000220751
Start 89769893:89769893(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.609delA
AA Mutation p.Lys203AsnfsTer36(p.K203Nfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000220751
Start 89789340:89789340(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1146delT
AA Mutation p.Phe382LeufsTer2(p.F382Lfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript