Primary Site >> Stomach Cancer

Gene >> KDM2A

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000529006
Start 67243009:67243009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1480A>G
AA Mutation p.Ile494Val(p.I494V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67253567:67253567(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3047A>G
AA Mutation p.Asp1016Gly(p.D1016G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67231781:67231781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1300C>T
AA Mutation p.His434Tyr(p.H434Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67254404:67254404(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3293A>G
AA Mutation p.Glu1098Gly(p.E1098G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67248366:67248366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2051C>G
AA Mutation p.Ala684Gly(p.A684G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67250737:67250737(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372925935
CDS Mutation c.2707C>T
AA Mutation p.Arg903Cys(p.R903C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67254918:67254918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3352A>G
AA Mutation p.Ile1118Val(p.I1118V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000529006
Start 67250273:67250273(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2243A>G
AA Mutation p.His748Arg(p.H748R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000529006
Start 67250697:67250697(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750239468
CDS Mutation c.2667C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000529006
Start 67250418:67250418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2388A>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000529006
Start 67250280:67250280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2250T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000529006
Start 67250607:67250607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2577A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000529006
Start 67250525:67250525(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2500delC
AA Mutation p.Arg834ValfsTer3(p.R834Vfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000529006
Start 67250101:67250101(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2071G>T
AA Mutation p.Glu691Ter(p.E691*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript