Primary Site >> Stomach Cancer

Gene >> NCAM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113207988:113207988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.902A>G
AA Mutation p.His301Arg(p.H301R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113233309:113233309(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1685C>A
AA Mutation p.Ala562Asp(p.A562D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113214416:113214416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964G>A
AA Mutation p.Glu322Lys(p.E322K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235102:113235102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1763C>T
AA Mutation p.Ala588Val(p.A588V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204414:113204414(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782428703
CDS Mutation c.256G>A
AA Mutation p.Ala86Thr(p.A86T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235135:113235135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs117485712
CDS Mutation c.1796C>T
AA Mutation p.Ala599Val(p.A599V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113260242:113260242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2050G>A
AA Mutation p.Val684Met(p.V684M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113204431:113204431(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.273C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113255959:113255959(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782154158
CDS Mutation c.1911C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113232289:113232289(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1360C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113202446:113202446(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782225091
CDS Mutation c.120A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113206143:113206143(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.591G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113233169:113233169(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782763937
CDS Mutation c.1545C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113207304:113207304(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782323015
CDS Mutation c.672C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113270342:113270342(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2286A>G
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000316851
Start 113233150:113233150(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1530delC
AA Mutation p.Ser511LeufsTer66(p.S511Lfs*66)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000316851
Start 113235164:113235164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1825C>T
AA Mutation p.Gln609Ter(p.Q609*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript