Primary Site >> Stomach Cancer

Gene >> SHH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155803657:155803657(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.632G>A
AA Mutation p.Gly211Asp(p.G211D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155806409:155806409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449C>T
AA Mutation p.Thr150Met(p.T150M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155806445:155806445(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413C>T
AA Mutation p.Ser138Phe(p.S138F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155811853:155811853(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.270A>C
AA Mutation p.Glu90Asp(p.E90D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155812086:155812086(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.37G>A
AA Mutation p.Val13Ile(p.V13I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000297261
Start 155806355:155806355(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.503C>T
AA Mutation p.Ala168Val(p.A168V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000297261
Start 155812066:155812066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.57C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000297261
Start 155803017:155803017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1272G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000297261
Start 155812099:155812099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.24G>A
Mutation Classification Silent
Feature Type Transcript