Primary Site >> Stomach Cancer

Gene >> HOXC6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000243108
Start 54029760:54029760(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.506G>A
AA Mutation p.Arg169His(p.R169H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000243108
Start 54029735:54029735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481C>A
AA Mutation p.His161Asn(p.H161N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000243108
Start 54028582:54028582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61C>T
AA Mutation p.Leu21Phe(p.L21F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000243108
Start 54029782:54029782(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61736613
CDS Mutation c.528C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000243108
Start 54029701:54029701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000243108
Start 54029785:54029785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.531G>A
Mutation Classification Silent
Feature Type Transcript