Primary Site >> Stomach Cancer

Gene >> MCM10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13171021:13171021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.107A>C
AA Mutation p.Asn36Thr(p.N36T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13175572:13175572(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150895215
CDS Mutation c.658C>T
AA Mutation p.Arg220Trp(p.R220W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13195117:13195117(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs74881009
CDS Mutation c.1825C>T
AA Mutation p.Arg609Trp(p.R609W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13182949:13182949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950T>G
AA Mutation p.Ile317Arg(p.I317R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13198764:13198764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2198A>G
AA Mutation p.Lys733Arg(p.K733R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000484800
Start 13186168:13186168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1106G>A
AA Mutation p.Cys369Tyr(p.C369Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000484800
Start 13171034:13171034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.120C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000484800
Start 13192491:13192491(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377010061
CDS Mutation c.1671G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000484800
Start 13175565:13175565(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs568860384
CDS Mutation c.651G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000484800
Start 13204329:13204329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2466C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000484800
Start 13204300:13204300(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2441delT
AA Mutation p.Phe814SerfsTer34(p.F814Sfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000484800
Start 13197741:13197741(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2102delA
AA Mutation p.Asn701ThrfsTer35(p.N701Tfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000484800
Start 13171236:13171236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.322C>T
AA Mutation p.Arg108Ter(p.R108*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant;coding_sequence_variant
Transcription ID ENST00000484800
Start 13183083:13183102(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1087_1101+5delGATGGTTCAGAGGAGGTAAG
Mutation Classification Splice_Site
Feature Type Transcript