Primary Site >> Stomach Cancer

Gene >> ACTA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88938101:88938101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950A>C
AA Mutation p.Lys317Thr(p.K317T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88939548:88939548(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.767G>A
AA Mutation p.Arg256His(p.R256H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88948918:88948918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13G>C
AA Mutation p.Glu5Gln(p.E5Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88941366:88941366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.479G>C
AA Mutation p.Gly160Ala(p.G160A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88948867:88948867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756496192
CDS Mutation c.64G>A
AA Mutation p.Gly22Ser(p.G22S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000224784
Start 88948816:88948816(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs112901682
CDS Mutation c.115C>T
AA Mutation p.Arg39Cys(p.R39C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000224784
Start 88941792:88941792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000224784
Start 88939532:88939532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.783G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000224784
Start 88938140:88938140(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.911delG
AA Mutation p.Gly304AlafsTer19(p.G304Afs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript