Primary Site >> Stomach Cancer

Gene >> ADGRL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81981846:81981846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3140T>A
AA Mutation p.Leu1047His(p.L1047H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990792:81990792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4027G>C
AA Mutation p.Val1343Leu(p.V1343L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990898:81990898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4133T>G
AA Mutation p.Leu1378Arg(p.L1378R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81936820:81936820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.380A>G
AA Mutation p.Tyr127Cys(p.Y127C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81952071:81952071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1711G>A
AA Mutation p.Asp571Asn(p.D571N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81837039:81837039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.55T>G
AA Mutation p.Phe19Val(p.F19V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81943424:81943424(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.853A>C
AA Mutation p.Met285Leu(p.M285L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81968189:81968189(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2501G>A
AA Mutation p.Arg834Lys(p.R834K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990592:81990592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200002945
CDS Mutation c.3827G>A
AA Mutation p.Ser1276Asn(p.S1276N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81966589:81966589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2317T>C
AA Mutation p.Phe773Leu(p.F773L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81970363:81970363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2771C>T
AA Mutation p.Ala924Val(p.A924V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81981972:81981972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3266A>G
AA Mutation p.Lys1089Arg(p.K1089R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990954:81990954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4189T>C
AA Mutation p.Ser1397Pro(p.S1397P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81991008:81991008(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770815631
CDS Mutation c.4243G>T
AA Mutation p.Ala1415Ser(p.A1415S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81979896:81979896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3037T>G
AA Mutation p.Leu1013Val(p.L1013V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990885:81990885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4120A>C
AA Mutation p.Ser1374Arg(p.S1374R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81990660:81990660(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751411562
CDS Mutation c.3895G>A
AA Mutation p.Asp1299Asn(p.D1299N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81970440:81970440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2848A>G
AA Mutation p.Lys950Glu(p.K950E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81955899:81955899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1844A>T
AA Mutation p.Asn615Ile(p.N615I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81985262:81985262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3403C>T
AA Mutation p.Arg1135Cys(p.R1135C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81907206:81907206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.263A>T
AA Mutation p.Asp88Val(p.D88V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000370717
Start 81950414:81950414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1424A>T
AA Mutation p.Lys475Met(p.K475M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000370717
Start 81950259:81950259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1269T>C
Mutation Classification Silent
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000370717
Start 81986992:81986992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3588A>G
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000370717
Start 81990866:81990866(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4101C>T
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000370717
Start 81943003:81943003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.432G>A
Mutation Classification Silent
Feature Type Transcript
ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000370717
Start 81907195:81907195(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.252C>T
Mutation Classification Silent
Feature Type Transcript
ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000370717
Start 81966550:81966551(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2279_2280delAA
AA Mutation p.Lys760ArgfsTer9(p.K760Rfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 29
Mutation Consequence stop_gained
Transcription ID ENST00000370717
Start 81943379:81943379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.808G>T
AA Mutation p.Glu270Ter(p.E270*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence stop_gained
Transcription ID ENST00000370717
Start 81966087:81966087(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2035G>T
AA Mutation p.Gly679Ter(p.G679*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000370717
Start 81981833:81981834(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3129dupT
AA Mutation p.Leu1044SerfsTer16(p.L1044Sfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript