Primary Site >> Stomach Cancer

Gene >> SP5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375281
Start 170716674:170716674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.467C>T
AA Mutation p.Pro156Leu(p.P156L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375281
Start 170717391:170717391(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1184C>T
AA Mutation p.Ala395Val(p.A395V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000375281
Start 170716318:170716318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.111C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375281
Start 170716444:170716444(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.237G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375281
Start 170717173:170717173(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.966C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000375281
Start 170716504:170716504(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764033975
CDS Mutation c.297G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375281
Start 170717206:170717206(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147780061
CDS Mutation c.999C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000375281
Start 170716515:170716533(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.310_328delTCCTTCGGGGCTGCGCACG
AA Mutation p.Gly106ProfsTer202(p.G106Pfs*202)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000375281
Start 170716373:170716373(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.166C>T
AA Mutation p.Gln56Ter(p.Q56*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript