Primary Site >> Stomach Cancer

Gene >> MIB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21864613:21864613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763759712
CDS Mutation c.2968A>T
AA Mutation p.Ser990Cys(p.S990C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21838468:21838468(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747233793
CDS Mutation c.1933G>A
AA Mutation p.Val645Ile(p.V645I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21791505:21791505(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781423306
CDS Mutation c.1040G>A
AA Mutation p.Arg347Gln(p.R347Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21815667:21815667(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374317020
CDS Mutation c.1531G>A
AA Mutation p.Ala511Thr(p.A511T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21773700:21773700(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.608A>G
AA Mutation p.Asn203Ser(p.N203S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261537
Start 21779552:21779552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.775G>A
AA Mutation p.Glu259Lys(p.E259K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261537
Start 21847051:21847051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2319T>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261537
Start 21838458:21838458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1923T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000261537
Start 21838392:21838392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1857A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000261537
Start 21803940:21803940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1405C>T
AA Mutation p.Gln469Ter(p.Q469*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000261537
Start 21791464:21791465(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.999_1000insTCCCCCTCTTCCCTTTGGAGCACTGA
AA Mutation p.Gln334SerfsTer42(p.Q334Sfs*42)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript