Primary Site >> Stomach Cancer

Gene >> HOXC11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000546378
Start 53973837:53973837(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.596C>T
AA Mutation p.Ala199Val(p.A199V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000546378
Start 53973315:53973315(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199765463
CDS Mutation c.74G>A
AA Mutation p.Arg25Gln(p.R25Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000546378
Start 53975250:53975250(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.752T>C
AA Mutation p.Phe251Ser(p.F251S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000546378
Start 53973646:53973646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.405C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000546378
Start 53973325:53973325(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.84C>T
Mutation Classification Silent
Feature Type Transcript