Primary Site >> Stomach Cancer

Gene >> ISYNA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338128
Start 18435782:18435782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1115C>T
AA Mutation p.Thr372Met(p.T372M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338128
Start 18437003:18437003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.385A>C
AA Mutation p.Met129Leu(p.M129L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338128
Start 18436740:18436740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.553G>A
AA Mutation p.Ala185Thr(p.A185T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338128
Start 18436436:18436436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138096546
CDS Mutation c.653C>T
AA Mutation p.Ala218Val(p.A218V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000338128
Start 18435656:18435656(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777014766
CDS Mutation c.1161G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000338128
Start 18436131:18436131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.876G>A
Mutation Classification Silent
Feature Type Transcript