Primary Site >> Stomach Cancer

Gene >> MPP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369534
Start 154792182:154792182(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.206T>C
AA Mutation p.Val69Ala(p.V69A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369534
Start 154792213:154792213(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175G>A
AA Mutation p.Ala59Thr(p.A59T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369534
Start 154791805:154791805(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374791319
CDS Mutation c.289G>A
AA Mutation p.Ala97Thr(p.A97T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369534
Start 154779182:154779182(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1396T>C
AA Mutation p.Tyr466His(p.Y466H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369534
Start 154781651:154781651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782259153
CDS Mutation c.1098G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence inframe_deletion
Transcription ID ENST00000369534
Start 154779327:154779329(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1249_1251delAAG
AA Mutation p.Lys417del(p.K417del)
Mutation Classification In_Frame_Del
Feature Type Transcript