Primary Site >> Stomach Cancer

Gene >> GRIN1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000371561
Start 137161414:137161414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1465C>T
AA Mutation p.Arg489Trp(p.R489W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137163792:137163792(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2477C>T
AA Mutation p.Ala826Val(p.A826V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137161144:137161144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1286A>G
AA Mutation p.Asp429Gly(p.D429G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137145747:137145747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.415C>T
AA Mutation p.Arg139Cys(p.R139C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137139724:137139724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748041860
CDS Mutation c.238G>A
AA Mutation p.Glu80Lys(p.E80K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137165280:137165280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2684G>T
AA Mutation p.Arg895Met(p.R895M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137149106:137149106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.668C>T
AA Mutation p.Ala223Val(p.A223V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000371561
Start 137156897:137156897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.828C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000371561
Start 137142044:137142044(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.294delC
AA Mutation p.Asn99ThrfsTer23(p.N99Tfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000371561
Start 137165189:137165192(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2596_2599delAAGA
AA Mutation p.Lys866ValfsTer188(p.K866Vfs*188)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000371561
Start 137163779:137163779(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2468delG
AA Mutation p.Gly823AlafsTer8(p.G823Afs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript