Primary Site >> Stomach Cancer

Gene >> ST7

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265437
Start 117130492:117130492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451T>C
AA Mutation p.Tyr151His(p.Y151H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265437
Start 117129808:117129808(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs528877219
CDS Mutation c.410G>A
AA Mutation p.Arg137Gln(p.R137Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265437
Start 117209870:117209870(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1338C>A
AA Mutation p.Phe446Leu(p.F446L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265437
Start 117170953:117170953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1055A>C
AA Mutation p.Gln352Pro(p.Q352P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000265437
Start 117209924:117209924(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761925373
CDS Mutation c.1392T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000265437
Start 117119716:117119716(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.390C>T
Mutation Classification Silent
Feature Type Transcript