Primary Site >> Stomach Cancer

Gene >> GPA33

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367868
Start 167055022:167055022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.781T>C
AA Mutation p.Cys261Arg(p.C261R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367868
Start 167055001:167055001(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.802A>G
AA Mutation p.Thr268Ala(p.T268A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367868
Start 167069072:167069072(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139630164
CDS Mutation c.265G>A
AA Mutation p.Val89Ile(p.V89I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000367868
Start 167055071:167055071(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752212756
CDS Mutation c.732C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000367868
Start 167055764:167055764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.657G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000367868
Start 167055065:167055065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.738T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000367868
Start 167054409:167054410(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.883_884dupAG
AA Mutation p.Glu296GlyfsTer81(p.E296Gfs*81)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript