Primary Site >> Stomach Cancer

Gene >> NOX4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89335888:89335888(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140266495
CDS Mutation c.1573C>T
AA Mutation p.Arg525Trp(p.R525W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89444155:89444155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.427G>A
AA Mutation p.Ala143Thr(p.A143T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000263317
Start 89340170:89340170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs55696571
CDS Mutation c.1339G>T
AA Mutation p.Asp447Tyr(p.D447Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89400280:89400280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.946A>C
AA Mutation p.Ser316Arg(p.S316R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89491227:89491227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.20G>C
AA Mutation p.Ser7Thr(p.S7T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89342096:89342096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315G>T
AA Mutation p.Ala439Ser(p.A439S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89491200:89491200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.47A>G
AA Mutation p.His16Arg(p.H16R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000263317
Start 89342079:89342079(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1332C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263317
Start 89326870:89326870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1623A>T
Mutation Classification Silent
Feature Type Transcript