Primary Site >> Stomach Cancer

Gene >> HSP90AB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44251469:44251469(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1175G>A
AA Mutation p.Arg392Gln(p.R392Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44249810:44249810(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.490T>G
AA Mutation p.Ser164Ala(p.S164A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44251100:44251100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1010G>A
AA Mutation p.Arg337His(p.R337H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44253199:44253199(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1886A>T
AA Mutation p.Asn629Ile(p.N629I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44251102:44251102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012C>T
AA Mutation p.Arg338Trp(p.R338W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44251507:44251507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1213C>T
AA Mutation p.Arg405Cys(p.R405C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000353801
Start 44252068:44252068(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1532T>C
AA Mutation p.Val511Ala(p.V511A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000353801
Start 44251182:44251182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1092C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000353801
Start 44248719:44248719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.90T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000353801
Start 44251509:44251510(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1220dupA
AA Mutation p.Asn407LysfsTer4(p.N407Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript