Primary Site >> Stomach Cancer

Gene >> CCT4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394440
Start 61872276:61872276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1297G>A
AA Mutation p.Ala433Thr(p.A433T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394440
Start 61872543:61872543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780849011
CDS Mutation c.1171C>T
AA Mutation p.Arg391Cys(p.R391C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394440
Start 61878947:61878947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs528619072
CDS Mutation c.444G>T
AA Mutation p.Leu148Phe(p.L148F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000394440
Start 61883534:61883534(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760718212
CDS Mutation c.195A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000394440
Start 61872247:61872247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375306467
CDS Mutation c.1326A>G
Mutation Classification Silent
Feature Type Transcript