Primary Site >> Stomach Cancer

Gene >> HOXB5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48592223:48592223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.796G>A
AA Mutation p.Ala266Thr(p.A266T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48592286:48592286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.733C>T
AA Mutation p.Arg245Trp(p.R245W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48592266:48592266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.753G>T
AA Mutation p.Lys251Asn(p.K251N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48593178:48593178(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.505C>T
AA Mutation p.Pro169Ser(p.P169S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48593528:48593528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777962205
CDS Mutation c.155T>C
AA Mutation p.Met52Thr(p.M52T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000239151
Start 48592453:48592453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.566T>C
AA Mutation p.Met189Thr(p.M189T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000239151
Start 48593281:48593281(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757733005
CDS Mutation c.402C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000239151
Start 48593359:48593359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.324C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000239151
Start 48593602:48593602(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000239151
Start 48593290:48593290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.393C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000239151
Start 48592440:48592440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.579C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000239151
Start 48592324:48592325(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.694dupT
AA Mutation p.Cys232LeufsTer106(p.C232Lfs*106)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript