Primary Site >> Stomach Cancer

Gene >> ADCYAP1R1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31063277:31063277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759359114
CDS Mutation c.13G>A
AA Mutation p.Val5Met(p.V5M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31092693:31092693(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1004T>G
AA Mutation p.Leu335Arg(p.L335R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31085327:31085327(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745856523
CDS Mutation c.554G>A
AA Mutation p.Arg185His(p.R185H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31106499:31106499(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1222C>A
AA Mutation p.Gln408Lys(p.Q408K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31106524:31106524(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766086000
CDS Mutation c.1247G>A
AA Mutation p.Arg416Gln(p.R416Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000304166
Start 31086519:31086519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805T>C
AA Mutation p.Tyr269His(p.Y269H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000304166
Start 31063288:31063288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.24C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000304166
Start 31063276:31063276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000304166
Start 31064831:31064832(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.56dupC
AA Mutation p.Ala20CysfsTer5(p.A20Cfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000304166
Start 31086952:31086953(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.842_843dupTG
AA Mutation p.Thr282Ter(p.T282*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript