Primary Site >> Stomach Cancer

Gene >> VPS37B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000267202
Start 122871010:122871010(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.163C>A
AA Mutation p.Leu55Met(p.L55M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000267202
Start 122896002:122896002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000267202
Start 122867371:122867371(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201537364
CDS Mutation c.603C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000267202
Start 122867436:122867436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.538C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000267202
Start 122867449:122867449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754778954
CDS Mutation c.525G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000267202
Start 122867409:122867409(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.565delC
AA Mutation p.Leu189PhefsTer31(p.L189Ffs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000267202
Start 122867440:122867440(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.534delC
AA Mutation p.Arg179GlyfsTer41(p.R179Gfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript