Primary Site >> Stomach Cancer

Gene >> ADORA3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369717
Start 111563909:111563909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.44G>T
AA Mutation p.Arg15Met(p.R15M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369717
Start 111488916:111488916(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780824295
CDS Mutation c.323G>A
AA Mutation p.Arg108Gln(p.R108Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000241356
Start 111500324:111500324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143962803
CDS Mutation c.583G>A
AA Mutation p.Ala195Thr(p.A195T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000241356
Start 111503009:111503009(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766923748
CDS Mutation c.346G>A
AA Mutation p.Val116Ile(p.V116I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369717
Start 111486605:111486605(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.610C>T
AA Mutation p.Arg204Cys(p.R204C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000241356
Start 111500216:111500216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.691T>G
AA Mutation p.Ser231Ala(p.S231A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000369717
Start 111488974:111488974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.265G>A
AA Mutation p.Ala89Thr(p.A89T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000369717
Start 111490672:111490672(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.198C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000241356
Start 111500207:111500207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.700C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000241356
Start 111503188:111503189(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.166_167insA
AA Mutation p.Leu56HisfsTer3(p.L56Hfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript