Primary Site >> Stomach Cancer

Gene >> CORO1A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30188500:30188500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1205G>A
AA Mutation p.Arg402Gln(p.R402Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30188404:30188404(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1109C>A
AA Mutation p.Pro370His(p.P370H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30185228:30185228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.19C>T
AA Mutation p.Arg7Cys(p.R7C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30187812:30187812(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.844G>A
AA Mutation p.Val282Ile(p.V282I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30188408:30188408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1113C>A
AA Mutation p.Asp371Glu(p.D371E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30188006:30188006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.926T>C
AA Mutation p.Met309Thr(p.M309T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000219150
Start 30187424:30187424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.679G>A
AA Mutation p.Val227Met(p.V227M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000219150
Start 30188369:30188369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1074G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000219150
Start 30188399:30188399(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1104A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000219150
Start 30186708:30186708(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000219150
Start 30186834:30186834(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.344delG
AA Mutation p.Gly115AlafsTer2(p.G115Afs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript