Primary Site >> Stomach Cancer

Gene >> ADHFE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66457112:66457112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1108A>G
AA Mutation p.Thr370Ala(p.T370A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66444613:66444613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.218C>T
AA Mutation p.Ala73Val(p.A73V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66456831:66456831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1001A>G
AA Mutation p.Tyr334Cys(p.Y334C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66444601:66444601(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755425165
CDS Mutation c.206A>G
AA Mutation p.Lys69Arg(p.K69R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66448937:66448937(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766239380
CDS Mutation c.701G>A
AA Mutation p.Arg234Gln(p.R234Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000396623
Start 66440163:66440163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61T>C
AA Mutation p.Cys21Arg(p.C21R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66451973:66451973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.755C>A
AA Mutation p.Thr252Asn(p.T252N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000396623
Start 66445288:66445288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424A>G
AA Mutation p.Thr142Ala(p.T142A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000396623
Start 66452073:66452073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.855C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000396623
Start 66452058:66452058(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.840C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000396623
Start 66457150:66457150(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1146G>A
Mutation Classification Silent
Feature Type Transcript