Primary Site >> Stomach Cancer

Gene >> THBD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377103
Start 23048321:23048321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759926568
CDS Mutation c.1184C>T
AA Mutation p.Ala395Val(p.A395V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377103
Start 23048977:23048977(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.528G>T
AA Mutation p.Arg176Ser(p.R176S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377103
Start 23048564:23048564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.941A>G
AA Mutation p.Tyr314Cys(p.Y314C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23047843:23047843(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1662C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23048551:23048551(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754792536
CDS Mutation c.954C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23048161:23048161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1344C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23048302:23048302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1203G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23048425:23048425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000377103
Start 23048428:23048428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1077C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000377103
Start 23048589:23048592(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.913_916delTCCT
AA Mutation p.Ser305ThrfsTer76(p.S305Tfs*76)
Mutation Classification Frame_Shift_Del
Feature Type Transcript