Primary Site >> Stomach Cancer

Gene >> CD1D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158181520:158181520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780562127
CDS Mutation c.127C>T
AA Mutation p.Arg43Cys(p.R43C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158183063:158183063(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.793G>A
AA Mutation p.Ala265Thr(p.A265T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158182130:158182130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.427A>C
AA Mutation p.Ser143Arg(p.S143R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158181527:158181527(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.134A>G
AA Mutation p.Asp45Gly(p.D45G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158182212:158182212(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.509A>C
AA Mutation p.Lys170Thr(p.K170T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158184020:158184020(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774424909
CDS Mutation c.971G>A
AA Mutation p.Arg324Gln(p.R324Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158183054:158183054(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.784T>C
AA Mutation p.Tyr262His(p.Y262H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158182935:158182935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.665T>G
AA Mutation p.Leu222Arg(p.L222R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158181700:158181700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.307G>A
AA Mutation p.Ala103Thr(p.A103T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158182173:158182173(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.470T>C
AA Mutation p.Leu157Pro(p.L157P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158182184:158182184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481T>G
AA Mutation p.Leu161Val(p.L161V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000368171
Start 158181688:158181688(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.295G>A
AA Mutation p.Val99Met(p.V99M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000368171
Start 158182252:158182252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.549C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000368171
Start 158181519:158181519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.126G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000368171
Start 158181579:158181579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.186G>A
Mutation Classification Silent
Feature Type Transcript