Primary Site >> Stomach Cancer

Gene >> TRIM63

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374272
Start 26058586:26058586(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.635A>C
AA Mutation p.Lys212Thr(p.K212T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374272
Start 26057280:26057280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.902G>A
AA Mutation p.Gly301Asp(p.G301D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000374272
Start 26058579:26058579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.642C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000374272
Start 26058402:26058402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.819C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000374272
Start 26053956:26053956(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.988G>T
AA Mutation p.Glu330Ter(p.E330*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000374272
Start 26058428:26058428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.793C>T
AA Mutation p.Gln265Ter(p.Q265*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript