Primary Site >> Stomach Cancer

Gene >> MCM5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35412561:35412561(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757968764
CDS Mutation c.971G>A
AA Mutation p.Arg324His(p.R324H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35406682:35406682(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142715814
CDS Mutation c.553C>T
AA Mutation p.Arg185Cys(p.R185C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35415898:35415898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768089056
CDS Mutation c.1273C>T
AA Mutation p.Arg425Trp(p.R425W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000216122
Start 35420011:35420011(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1831C>T
AA Mutation p.Arg611Trp(p.R611W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35408517:35408517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.706G>A
AA Mutation p.Val236Ile(p.V236I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35406628:35406628(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181776514
CDS Mutation c.499C>T
AA Mutation p.Arg167Cys(p.R167C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35410788:35410788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.797T>C
AA Mutation p.Met266Thr(p.M266T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000216122
Start 35416355:35416355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1364G>A
AA Mutation p.Arg455His(p.R455H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000216122
Start 35412661:35412661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1071C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000216122
Start 35408525:35408525(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.714C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000216122
Start 35421317:35421317(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1833-1G>T
Mutation Classification Splice_Site
Feature Type Transcript