Primary Site >> Stomach Cancer

Gene >> CD1C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292617:158292617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.632C>T
AA Mutation p.Ser211Phe(p.S211F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292617:158292617(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.632C>A
AA Mutation p.Ser211Tyr(p.S211Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292649:158292649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.664T>A
AA Mutation p.Leu222Met(p.L222M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158291227:158291227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.155A>T
AA Mutation p.Glu52Val(p.E52V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158293278:158293278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.956T>A
AA Mutation p.Leu319His(p.L319H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158291387:158291387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.315A>T
AA Mutation p.Gln105His(p.Q105H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292229:158292229(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.474G>T
AA Mutation p.Leu158Phe(p.L158F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292858:158292858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.873C>A
AA Mutation p.Asp291Glu(p.D291E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292622:158292622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.637C>A
AA Mutation p.Arg213Ser(p.R213S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292095:158292095(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.340G>T
AA Mutation p.Val114Leu(p.V114L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000368170
Start 158292345:158292345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.590A>T
AA Mutation p.Lys197Met(p.K197M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000368170
Start 158292852:158292852(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.867C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000368170
Start 158290079:158290079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.15G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000368170
Start 158292097:158292097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342A>G
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000368170
Start 158291351:158291351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence splice_donor_variant
Transcription ID ENST00000368170
Start 158290126:158290126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61+1G>C
Mutation Classification Splice_Site
Feature Type Transcript