Primary Site >> Stomach Cancer

Gene >> AP4B1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113895435:113895435(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776964406
CDS Mutation c.1850C>A
AA Mutation p.Ala617Asp(p.A617D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113896456:113896456(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1312G>T
AA Mutation p.Ala438Ser(p.A438S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113900081:113900081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.937A>G
AA Mutation p.Ser313Gly(p.S313G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113895277:113895277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs528147130
CDS Mutation c.2008G>A
AA Mutation p.Ala670Thr(p.A670T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113895933:113895933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1616A>G
AA Mutation p.Asp539Gly(p.D539G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113895114:113895114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2171T>A
AA Mutation p.Ile724Asn(p.I724N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113899946:113899946(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1072G>T
AA Mutation p.Asp358Tyr(p.D358Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113904697:113904697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.21G>T
AA Mutation p.Glu7Asp(p.E7D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000256658
Start 113900293:113900293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.725G>T
AA Mutation p.Ser242Ile(p.S242I)
Mutation Classification Missense_Mutation
Feature Type Transcript