Primary Site >> Stomach Cancer

Gene >> NOL8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92315564:92315564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1061T>C
AA Mutation p.Leu354Ser(p.L354S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92315004:92315004(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1621C>A
AA Mutation p.Pro541Thr(p.P541T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92314431:92314431(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758309678
CDS Mutation c.2194C>T
AA Mutation p.Arg732Trp(p.R732W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92315018:92315018(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372982099
CDS Mutation c.1607G>A
AA Mutation p.Arg536Gln(p.R536Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92314833:92314833(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1792A>G
AA Mutation p.Lys598Glu(p.K598E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92315322:92315322(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201001874
CDS Mutation c.1303G>A
AA Mutation p.Glu435Lys(p.E435K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92314802:92314802(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1823C>A
AA Mutation p.Pro608His(p.P608H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92311174:92311174(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2444A>G
AA Mutation p.Gln815Arg(p.Q815R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92299970:92299970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3222G>T
AA Mutation p.Gln1074His(p.Q1074H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000442668
Start 92311171:92311171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2447G>C
AA Mutation p.Ser816Thr(p.S816T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000442668
Start 92315263:92315263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1362T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000442668
Start 92314324:92314324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763859897
CDS Mutation c.2301G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000442668
Start 92301579:92301579(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3147delT
AA Mutation p.Phe1049LeufsTer8(p.F1049Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000442668
Start 92314315:92314315(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2310delA
AA Mutation p.Ala771GlnfsTer53(p.A771Qfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000442668
Start 92306973:92306973(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2738delA
AA Mutation p.Lys913ArgfsTer4(p.K913Rfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000442668
Start 92314314:92314315(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2310dupA
AA Mutation p.Ala771SerfsTer11(p.A771Sfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000442668
Start 92324211:92324211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.-48-2A>G
Mutation Classification Splice_Site
Feature Type Transcript