Primary Site >> Stomach Cancer

Gene >> PDE4D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000340635
Start 58977201:58977201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1697T>C
AA Mutation p.Val566Ala(p.V566A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000340635
Start 58974981:58974981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2113C>T
AA Mutation p.Arg705Cys(p.R705C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000340635
Start 59038875:59038875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.905A>G
AA Mutation p.Glu302Gly(p.E302G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000502484
Start 59988521:59988521(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771006931
CDS Mutation c.239C>T
AA Mutation p.Pro80Leu(p.P80L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000502484
Start 59988629:59988629(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774486077
CDS Mutation c.131G>A
AA Mutation p.Arg44His(p.R44H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000340635
Start 58991841:58991841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1179C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000340635
Start 58974808:58974808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2286C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000340635
Start 58991924:58991924(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1096G>T
AA Mutation p.Gly366Ter(p.G366*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript