Primary Site >> Stomach Cancer

Gene >> CDKL5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18650523:18650523(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2911G>A
AA Mutation p.Gly971Ser(p.G971S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18628527:18628527(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs398123694
CDS Mutation c.2653G>A
AA Mutation p.Gly885Arg(p.G885R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18603987:18603987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1063C>T
AA Mutation p.Arg355Trp(p.R355W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18584332:18584332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267606715
CDS Mutation c.533G>A
AA Mutation p.Arg178Gln(p.R178Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18628506:18628506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2632C>T
AA Mutation p.Pro878Ser(p.P878S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18579905:18579905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.340A>G
AA Mutation p.Ser114Gly(p.S114G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379989
Start 18604657:18604657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1733A>G
AA Mutation p.Asp578Gly(p.D578G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379989
Start 18584288:18584288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.489C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379989
Start 18604595:18604595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1671A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000379989
Start 18653472:18653472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3021G>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000379989
Start 18604454:18604454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1530G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000379989
Start 18604286:18604286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1362A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000379989
Start 18603930:18603930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1006C>T
AA Mutation p.Gln336Ter(p.Q336*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript