Primary Site >> Stomach Cancer

Gene >> LRP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12159062:12159062(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs572509429
CDS Mutation c.2558G>A
AA Mutation p.Arg853His(p.R853H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12147503:12147503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3260C>A
AA Mutation p.Ala1087Asp(p.A1087D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12181394:12181394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759106535
CDS Mutation c.1022G>A
AA Mutation p.Arg341His(p.R341H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12147380:12147380(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755158176
CDS Mutation c.3383G>A
AA Mutation p.Ser1128Asn(p.S1128N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12181132:12181132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284A>C
AA Mutation p.Glu428Asp(p.E428D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12162296:12162296(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2176A>G
AA Mutation p.Thr726Ala(p.T726A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12187039:12187039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.728G>A
AA Mutation p.Ser243Asn(p.S243N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12181259:12181259(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371768750
CDS Mutation c.1157G>A
AA Mutation p.Arg386His(p.R386H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261349
Start 12150990:12150990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2840T>A
AA Mutation p.Met947Lys(p.M947K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant;stop_lost
Transcription ID ENST00000261349
Start 12121126:12121130(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4838_4842delCCTGA
AA Mutation p.Ser1613Trp(p.S1613W)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000261349
Start 12164395:12164395(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1930C>T
AA Mutation p.Arg644Ter(p.R644*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000261349
Start 12125361:12125361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4384C>T
AA Mutation p.Arg1462Ter(p.R1462*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript