Primary Site >> Stomach Cancer

Gene >> ALDOB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101430804:101430804(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.84G>T
AA Mutation p.Lys28Asn(p.K28N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101430850:101430850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.38A>C
AA Mutation p.Lys13Thr(p.K13T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101425003:101425003(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.839C>T
AA Mutation p.Ala280Val(p.A280V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101430815:101430815(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.73G>A
AA Mutation p.Ala25Thr(p.A25T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101424973:101424973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869G>T
AA Mutation p.Cys290Phe(p.C290F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101425620:101425620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.632C>T
AA Mutation p.Ala211Val(p.A211V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101427501:101427501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.521A>G
AA Mutation p.Tyr174Cys(p.Y174C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000374855
Start 101424887:101424887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.955G>A
AA Mutation p.Ala319Thr(p.A319T)
Mutation Classification Missense_Mutation
Feature Type Transcript