Primary Site >> Stomach Cancer

Gene >> FANCB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324138
Start 14865420:14865420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.91A>C
AA Mutation p.Asn31His(p.N31H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324138
Start 14864966:14864966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.545T>G
AA Mutation p.Val182Gly(p.V182G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324138
Start 14844613:14844613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2055C>G
AA Mutation p.Ile685Met(p.I685M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324138
Start 14857899:14857899(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757202355
CDS Mutation c.1160G>A
AA Mutation p.Arg387His(p.R387H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324138
Start 14845165:14845165(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144205393
CDS Mutation c.1618T>G
AA Mutation p.Leu540Val(p.L540V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000324138
Start 14853123:14853123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1242T>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000324138
Start 14853111:14853111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1254T>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000324138
Start 14865205:14865205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000324138
Start 14865112:14865112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000324138
Start 14844918:14844918(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1865delT
AA Mutation p.Leu622Ter(p.L622*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000324138
Start 14853109:14853110(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1255_1256insCT
AA Mutation p.Ile419ThrfsTer9(p.I419Tfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000324138
Start 14844917:14844918(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1865dupT
AA Mutation p.Leu622PhefsTer36(p.L622Ffs*36)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript