Primary Site >> Stomach Cancer

Gene >> ACVR2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000241416
Start 147845184:147845184(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.32T>A
AA Mutation p.Val11Asp(p.V11D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000241416
Start 147922997:147922997(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1102C>T
AA Mutation p.Pro368Ser(p.P368S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000241416
Start 147927178:147927178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1446G>A
AA Mutation p.Met482Ile(p.M482I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000241416
Start 147917377:147917377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.767G>A
AA Mutation p.Gly256Asp(p.G256D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000241416
Start 147915302:147915302(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770920471
CDS Mutation c.640G>A
AA Mutation p.Glu214Lys(p.E214K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000241416
Start 147927124:147927124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1392C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000241416
Start 147926117:147926117(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs764719749
CDS Mutation c.1310delA
AA Mutation p.Lys437ArgfsTer5(p.K437Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000241416
Start 147899472:147899472(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.285delA
AA Mutation p.Asp96ThrfsTer54(p.D96Tfs*54)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000241416
Start 147923039:147923039(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1148delT
AA Mutation p.Leu383Ter(p.L383*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000241416
Start 147845172:147845172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.20T>A
AA Mutation p.Leu7Ter(p.L7*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000241416
Start 147896500:147896500(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.255C>A
AA Mutation p.Cys85Ter(p.C85*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript