Primary Site >> Stomach Cancer

Gene >> CDC25A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302506
Start 48183019:48183019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.339G>C
AA Mutation p.Leu113Phe(p.L113F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302506
Start 48165859:48165859(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1064A>C
AA Mutation p.Gln355Pro(p.Q355P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302506
Start 48164355:48164355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1274T>C
AA Mutation p.Val425Ala(p.V425A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302506
Start 48165731:48165731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096G>A
AA Mutation p.Ala366Thr(p.A366T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000302506
Start 48184664:48184664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000302506
Start 48159442:48159442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1336A>T
AA Mutation p.Arg446Ter(p.R446*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript