Primary Site >> Stomach Cancer

Gene >> STAT5B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42217393:42217393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1241C>T
AA Mutation p.Ala414Val(p.A414V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42219788:42219788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.605C>T
AA Mutation p.Thr202Met(p.T202M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42218862:42218862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.850G>A
AA Mutation p.Glu284Lys(p.E284K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42202802:42202802(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200333924
CDS Mutation c.2084C>T
AA Mutation p.Ala695Val(p.A695V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42216051:42216051(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1436C>T
AA Mutation p.Thr479Met(p.T479M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42223538:42223538(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.394A>G
AA Mutation p.Ser132Gly(p.S132G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42227642:42227642(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.172A>C
AA Mutation p.Thr58Pro(p.T58P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42218263:42218263(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762833594
CDS Mutation c.1057C>T
AA Mutation p.Arg353Cys(p.R353C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42223499:42223499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.433A>G
AA Mutation p.Asn145Asp(p.N145D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42223459:42223459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.473C>T
AA Mutation p.Thr158Ile(p.T158I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000293328
Start 42210271:42210271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1806G>T
AA Mutation p.Gln602His(p.Q602H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000293328
Start 42217431:42217431(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200710135
CDS Mutation c.1203C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000293328
Start 42210429:42210429(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1749delA
AA Mutation p.Lys583AsnfsTer16(p.K583Nfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000293328
Start 42223441:42223441(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.491delA
AA Mutation p.Lys164SerfsTer17(p.K164Sfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000293328
Start 42227582:42227582(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.232delG
AA Mutation p.Glu78LysfsTer6(p.E78Kfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000293328
Start 42210428:42210429(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1749dupA
AA Mutation p.His584ThrfsTer8(p.H584Tfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript