Primary Site >> Stomach Cancer

Gene >> ATP6AP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154433667:154433667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.631A>G
AA Mutation p.Lys211Glu(p.K211E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154435396:154435396(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1094G>A
AA Mutation p.Ser365Asn(p.S365N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154435390:154435390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1088G>A
AA Mutation p.Gly363Glu(p.G363E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154435842:154435842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1364G>A
AA Mutation p.Arg455His(p.R455H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154432308:154432308(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782516905
CDS Mutation c.406G>A
AA Mutation p.Val136Ile(p.V136I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369762
Start 154435772:154435772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1294A>G
AA Mutation p.Thr432Ala(p.T432A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000369762
Start 154433645:154433645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.609C>A
Mutation Classification Silent
Feature Type Transcript