Primary Site >> Stomach Cancer

Gene >> DNAJC14

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55828061:55828061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.598C>T
AA Mutation p.Arg200Cys(p.R200C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55828640:55828640(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769086235
CDS Mutation c.19G>A
AA Mutation p.Gly7Arg(p.G7R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55828222:55828222(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437G>T
AA Mutation p.Gly146Val(p.G146V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55827347:55827347(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1312C>G
AA Mutation p.Pro438Ala(p.P438A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55822012:55822012(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762110639
CDS Mutation c.2074C>T
AA Mutation p.Arg692Trp(p.R692W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55828574:55828574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85G>A
AA Mutation p.Val29Met(p.V29M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000317269
Start 55827862:55827862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.797T>C
AA Mutation p.Val266Ala(p.V266A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55822103:55822103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1983G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55827507:55827507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1152C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55822468:55822468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1803T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55827273:55827273(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1386C>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55828188:55828188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.471T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000317269
Start 55823102:55823102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1602T>C
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000317269
Start 55828420:55828420(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.239delG
AA Mutation p.Gly80ValfsTer176(p.G80Vfs*176)
Mutation Classification Frame_Shift_Del
Feature Type Transcript