Primary Site >> Stomach Cancer

Gene >> ING1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375774
Start 110719577:110719577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.914C>T
AA Mutation p.Ala305Val(p.A305V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375774
Start 110719667:110719667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1004C>T
AA Mutation p.Ala335Val(p.A335V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375774
Start 110719397:110719397(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.734G>A
AA Mutation p.Arg245His(p.R245H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375774
Start 110719605:110719605(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773617626
CDS Mutation c.942C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375774
Start 110719680:110719680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1017A>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000375774
Start 110715644:110715644(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.201T>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375774
Start 110719599:110719599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.936C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000375774
Start 110719725:110719725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1062G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000375774
Start 110719678:110719678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1015C>T
AA Mutation p.Arg339Ter(p.R339*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript