Primary Site >> Stomach Cancer

Gene >> ACVR1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51980990:51980990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.602G>A
AA Mutation p.Arg201His(p.R201H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51994043:51994043(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1451G>A
AA Mutation p.Arg484His(p.R484H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51986892:51986892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1211A>G
AA Mutation p.Tyr404Cys(p.Y404C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51991959:51991959(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1358G>A
AA Mutation p.Arg453His(p.R453H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51975379:51975379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.206G>A
AA Mutation p.Cys69Tyr(p.C69Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000257963
Start 51985230:51985230(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1018A>C
AA Mutation p.Asn340His(p.N340H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000257963
Start 51994050:51994050(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776085590
CDS Mutation c.1458G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000257963
Start 51951823:51951823(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.85delG
AA Mutation p.Val29SerfsTer57(p.V29Sfs*57)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000257963
Start 51981056:51981056(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.671delG
AA Mutation p.Gly224AlafsTer10(p.G224Afs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000257963
Start 51984100:51984100(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.913delA
AA Mutation p.Ile305LeufsTer32(p.I305Lfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000257963
Start 51985337:51985337(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1128delG
AA Mutation p.Thr377ProfsTer16(p.T377Pfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000257963
Start 51985212:51985212(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1000C>T
AA Mutation p.Arg334Ter(p.R334*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000257963
Start 51991931:51991931(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1330C>T
AA Mutation p.Arg444Ter(p.R444*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript