Primary Site >> Stomach Cancer

Gene >> GPNMB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000381990
Start 23260677:23260677(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.922A>G
AA Mutation p.Thr308Ala(p.T308A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000381990
Start 23246886:23246886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.29T>G
AA Mutation p.Phe10Cys(p.F10C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000381990
Start 23256987:23256987(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200717222
CDS Mutation c.463G>A
AA Mutation p.Val155Ile(p.V155I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000381990
Start 23267969:23267969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1237G>C
AA Mutation p.Val413Leu(p.V413L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000381990
Start 23257056:23257056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532C>A
AA Mutation p.His178Asn(p.H178N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000381990
Start 23253380:23253380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.144T>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000381990
Start 23270072:23270072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1362G>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000381990
Start 23266518:23266518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1056A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000381990
Start 23254260:23254260(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.315C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000381990
Start 23260550:23260550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.795C>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000381990
Start 23260754:23260754(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1002delA
AA Mutation p.Lys334AsnfsTer6(p.K334Nfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000381990
Start 23253444:23253444(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.212delA
AA Mutation p.Asn71ThrfsTer12(p.N71Tfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript