Primary Site >> Stomach Cancer

Gene >> ETF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360541
Start 138508326:138508326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1293T>G
AA Mutation p.Phe431Leu(p.F431L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360541
Start 138508815:138508815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085C>T
AA Mutation p.Thr362Ile(p.T362I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360541
Start 138517697:138517697(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.266C>T
AA Mutation p.Pro89Leu(p.P89L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360541
Start 138518745:138518745(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.209C>T
AA Mutation p.Ser70Leu(p.S70L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360541
Start 138512922:138512922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.574C>T
AA Mutation p.Arg192Cys(p.R192C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000360541
Start 138508329:138508329(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1290A>G
Mutation Classification Silent
Feature Type Transcript