Primary Site >> Stomach Cancer

Gene >> GH2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000423893
Start 63880839:63880839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.389G>A
AA Mutation p.Gly130Asp(p.G130D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000423893
Start 63881475:63881475(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760386827
CDS Mutation c.55T>C
AA Mutation p.Ser19Pro(p.S19P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000423893
Start 63880435:63880435(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771150182
CDS Mutation c.540C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000423893
Start 63881500:63881500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.30C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000423893
Start 63880883:63880883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.345C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000423893
Start 63880336:63880336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.639C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000423893
Start 63880793:63880793(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.435delA
AA Mutation p.Gly146AlafsTer5(p.G146Afs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript