Primary Site >> Stomach Cancer

Gene >> LIN28B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000345080
Start 105026407:105026407(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.308G>T
AA Mutation p.Gly103Val(p.G103V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000345080
Start 105026468:105026468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.369A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000345080
Start 105078600:105078600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.570T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000345080
Start 105078621:105078621(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141067774
CDS Mutation c.591C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000345080
Start 105026361:105026361(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.267delA
AA Mutation p.Lys89AsnfsTer11(p.K89Nfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript