Primary Site >> Stomach Cancer

Gene >> ADAM29

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174977396:174977396(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1871A>T
AA Mutation p.Asn624Ile(p.N624I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174977495:174977495(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1970G>T
AA Mutation p.Gly657Val(p.G657V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174975944:174975944(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.419C>T
AA Mutation p.Ala140Val(p.A140V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174977129:174977129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1604G>A
AA Mutation p.Gly535Asp(p.G535D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174977167:174977167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1642G>T
AA Mutation p.Asp548Tyr(p.D548Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174977684:174977684(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2159A>C
AA Mutation p.Lys720Thr(p.K720T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174976334:174976334(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.809G>A
AA Mutation p.Cys270Tyr(p.C270Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359240
Start 174976985:174976985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1460G>A
AA Mutation p.Cys487Tyr(p.C487Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000359240
Start 174976839:174976839(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755821340
CDS Mutation c.1314T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000359240
Start 174976635:174976635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1110T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000359240
Start 174975792:174975792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.267C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359240
Start 174975549:174975549(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.24T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000359240
Start 174977524:174977524(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2003delC
AA Mutation p.Pro668LeufsTer37(p.P668Lfs*37)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000359240
Start 174977619:174977620(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2101dupA
AA Mutation p.Ser701LysfsTer2(p.S701Kfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000359240
Start 174977165:174977166(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1641dupA
AA Mutation p.Asp548ArgfsTer10(p.D548Rfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript