Primary Site >> Liver Cancer

Gene >> TMEM132D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129074809:129074809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2366G>A
AA Mutation p.Gly789Glu(p.G789E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129084658:129084658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1488G>T
AA Mutation p.Met496Ile(p.M496I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129700545:129700545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.233G>A
AA Mutation p.Arg78Gln(p.R78Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129700068:129700068(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.710G>T
AA Mutation p.Gly237Val(p.G237V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129531124:129531124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1050T>A
AA Mutation p.Asp350Glu(p.D350E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129700108:129700108(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781773967
CDS Mutation c.670G>A
AA Mutation p.Val224Met(p.V224M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000422113
Start 129700612:129700612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.166G>A
AA Mutation p.Ala56Thr(p.A56T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000422113
Start 129073977:129073977(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3198G>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence splice_donor_variant
Transcription ID ENST00000422113
Start 129081757:129081757(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1923+2T>C
Mutation Classification Splice_Site
Feature Type Transcript