Primary Site >> Stomach Cancer

Gene >> ZNRF3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29050690:29050690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2509G>C
AA Mutation p.Asp837His(p.D837H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29050832:29050832(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2651C>T
AA Mutation p.Ala884Val(p.A884V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29049293:29049293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780878740
CDS Mutation c.1112G>A
AA Mutation p.Arg371His(p.R371H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29044841:29044841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.695T>C
AA Mutation p.Val232Ala(p.V232A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29048417:29048417(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372481492
CDS Mutation c.941G>A
AA Mutation p.Arg314Gln(p.R314Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29049308:29049308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1127A>T
AA Mutation p.Asn376Ile(p.N376I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29050529:29050529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2348A>C
AA Mutation p.Glu783Ala(p.E783A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29048395:29048395(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919C>T
AA Mutation p.Arg307Trp(p.R307W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000544604
Start 29048473:29048473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.997T>C
AA Mutation p.Cys333Arg(p.C333R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000544604
Start 29048433:29048433(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752839337
CDS Mutation c.957C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000544604
Start 29049411:29049411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1230G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000544604
Start 29050272:29050272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2091C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000544604
Start 29049309:29049309(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1128C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000544604
Start 29049351:29049351(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1170C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000544604
Start 29050549:29050549(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2372delG
AA Mutation p.Gly791AlafsTer14(p.G791Afs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000544604
Start 29050287:29050287(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2111delG
AA Mutation p.Gly704AlafsTer69(p.G704Afs*69)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000544604
Start 29050623:29050623(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2442delA
AA Mutation p.Pro815ArgfsTer11(p.P815Rfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000544604
Start 29050011:29050011(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1835delG
AA Mutation p.Gly612AlafsTer54(p.G612Afs*54)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 19
Mutation Consequence stop_gained
Transcription ID ENST00000544604
Start 29044879:29044879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733C>T
AA Mutation p.Arg245Ter(p.R245*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000544604
Start 29050756:29050756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2575C>T
AA Mutation p.Arg859Ter(p.R859*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence stop_gained
Transcription ID ENST00000544604
Start 29042501:29042501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433C>T
AA Mutation p.Arg145Ter(p.R145*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000544604
Start 28987170:28987171(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.398dupC
AA Mutation p.Lys134GlufsTer24(p.K134Efs*24)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript