Primary Site >> Stomach Cancer

Gene >> AVPR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000337474
Start 153906260:153906260(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61733407
CDS Mutation c.754C>T
AA Mutation p.Arg252Trp(p.R252W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000337474
Start 153906693:153906693(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782297695
CDS Mutation c.1081G>A
AA Mutation p.Ala361Thr(p.A361T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000337474
Start 153906526:153906526(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138974323
CDS Mutation c.914C>T
AA Mutation p.Ala305Val(p.A305V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000337474
Start 153906525:153906525(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145953185
CDS Mutation c.913G>A
AA Mutation p.Ala305Thr(p.A305T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000337474
Start 153906114:153906114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.608G>A
AA Mutation p.Arg203His(p.R203H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000337474
Start 153905170:153905170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368567969
CDS Mutation c.25G>A
AA Mutation p.Ala9Thr(p.A9T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000337474
Start 153905768:153905768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.262G>A
AA Mutation p.Val88Met(p.V88M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000337474
Start 153906304:153906304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.798G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000337474
Start 153905659:153905659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.153G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000337474
Start 153906239:153906239(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.738delG
AA Mutation p.Arg247AlafsTer24(p.R247Afs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000337474
Start 153906413:153906428(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.908_910+13delAAGGTGGGTGTAGCCG
Mutation Classification Splice_Site
Feature Type Transcript