Primary Site >> Stomach Cancer

Gene >> CSPG5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47569220:47569220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759344131
CDS Mutation c.1390C>T
AA Mutation p.Arg464Trp(p.R464W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47577859:47577859(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.167C>T
AA Mutation p.Ala56Val(p.A56V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47569123:47569123(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753978295
CDS Mutation c.1487C>T
AA Mutation p.Thr496Ile(p.T496I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47577245:47577245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.781G>A
AA Mutation p.Asp261Asn(p.D261N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47576951:47576951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1075T>C
AA Mutation p.Cys359Arg(p.C359R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47572837:47572837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1231C>T
AA Mutation p.Arg411Cys(p.R411C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000383738
Start 47577364:47577364(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.662G>A
AA Mutation p.Arg221His(p.R221H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000383738
Start 47562714:47562714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1587C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000383738
Start 47577675:47577675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.351C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000383738
Start 47577576:47577576(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.450C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000383738
Start 47577027:47577027(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.999delC
AA Mutation p.Gly334AlafsTer60(p.G334Afs*60)
Mutation Classification Frame_Shift_Del
Feature Type Transcript