Primary Site >> Stomach Cancer

Gene >> ACVR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263640
Start 157778172:157778172(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764097240
CDS Mutation c.502G>A
AA Mutation p.Glu168Lys(p.E168K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263640
Start 157799436:157799436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.58A>G
AA Mutation p.Ser20Gly(p.S20G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263640
Start 157737554:157737554(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769751827
CDS Mutation c.1507G>A
AA Mutation p.Asp503Asn(p.D503N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263640
Start 157778252:157778252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.422T>A
AA Mutation p.Leu141Gln(p.L141Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263640
Start 157770385:157770385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.773G>T
AA Mutation p.Arg258Met(p.R258M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000263640
Start 157780410:157780410(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.258C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000263640
Start 157737594:157737594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1467G>T
Mutation Classification Silent
Feature Type Transcript