Primary Site >> Stomach Cancer

Gene >> NBN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89981443:89981443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.252G>T
AA Mutation p.Gln84His(p.Q84H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89953303:89953303(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1786G>A
AA Mutation p.Asp596Asn(p.D596N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89980843:89980843(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781671474
CDS Mutation c.371G>A
AA Mutation p.Gly124Glu(p.G124E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89953447:89953447(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772234785
CDS Mutation c.1642A>G
AA Mutation p.Asn548Asp(p.N548D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89946185:89946185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2025A>G
AA Mutation p.Ile675Met(p.I675M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265433
Start 89937075:89937075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2185G>A
AA Mutation p.Val729Ile(p.V729I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89958839:89958839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1010C>T
AA Mutation p.Thr337Ile(p.T337I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89964440:89964440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964T>C
AA Mutation p.Tyr322His(p.Y322H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000265433
Start 89978263:89978263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.541C>A
AA Mutation p.Leu181Met(p.L181M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000265433
Start 89971230:89971230(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.645G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000265433
Start 89970540:89970540(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781323381
CDS Mutation c.720C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000265433
Start 89978288:89978288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.516A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000265433
Start 89953438:89953438(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1651delA
AA Mutation p.Arg551GlyfsTer8(p.R551Gfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000265433
Start 89955284:89955284(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1396delA
AA Mutation p.Arg466GlyfsTer18(p.R466Gfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000265433
Start 89946252:89946252(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1958delA
AA Mutation p.Lys653SerfsTer4(p.K653Sfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000265433
Start 89937028:89937028(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2232delT
AA Mutation p.Phe744LeufsTer7(p.F744Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000265433
Start 89981448:89981448(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.247delA
AA Mutation p.Met83CysfsTer9(p.M83Cfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript