Primary Site >> Stomach Cancer

Gene >> HSPA5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324460
Start 125238230:125238230(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1313C>A
AA Mutation p.Pro438Gln(p.P438Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324460
Start 125239306:125239306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.631C>A
AA Mutation p.Leu211Met(p.L211M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000324460
Start 125236955:125236955(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1602A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000324460
Start 125236778:125236778(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1779C>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000324460
Start 125236640:125236640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1917C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000324460
Start 125239031:125239031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.906G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000324460
Start 125241013:125241013(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.114C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000324460
Start 125239288:125239288(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.649delG
AA Mutation p.Glu217ArgfsTer76(p.E217Rfs*76)
Mutation Classification Frame_Shift_Del
Feature Type Transcript