Primary Site >> Stomach Cancer

Gene >> KCNIP3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95382387:95382387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566C>T
AA Mutation p.Ala189Val(p.A189V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95374385:95374385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.271A>G
AA Mutation p.Lys91Glu(p.K91E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95310413:95310413(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.74G>A
AA Mutation p.Ser25Asn(p.S25N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95374310:95374310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.196G>A
AA Mutation p.Glu66Lys(p.E66K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95381682:95381682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.534G>T
AA Mutation p.Lys178Asn(p.K178N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295225
Start 95375191:95375191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.430G>A
AA Mutation p.Gly144Arg(p.G144R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000295225
Start 95374352:95374368(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.243_259delGCTGCAGGCCCAGACCA
AA Mutation p.Leu82ValfsTer14(p.L82Vfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript