Primary Site >> Liver Cancer

Gene >> GRIN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137162973:137162973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2141C>G
AA Mutation p.Ala714Gly(p.A714G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137162650:137162650(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1924A>G
AA Mutation p.Ile642Val(p.I642V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137142071:137142071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.317C>T
AA Mutation p.Pro106Leu(p.P106L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000371561
Start 137161925:137161925(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1469T>C
AA Mutation p.Val490Ala(p.V490A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000371561
Start 137163666:137163666(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2441C>A
AA Mutation p.Ala814Asp(p.A814D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137145784:137145784(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.452G>T
AA Mutation p.Trp151Leu(p.W151L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371561
Start 137156706:137156706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.709A>G
AA Mutation p.Met237Val(p.M237V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence inframe_insertion
Transcription ID ENST00000371561
Start 137162974:137162975(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2143_2144insAAAAGAGAGATCAGATTGTTACTGTCTATG
AA Mutation p.Ala714_Ala715insGluLysArgAspGlnIleValThrValTyr(p.A714_A715insEKRDQIVTVY)
Mutation Classification In_Frame_Ins
Feature Type Transcript