Primary Site >> Stomach Cancer

Gene >> TAT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355962
Start 71568220:71568220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750638957
CDS Mutation c.1289C>T
AA Mutation p.Ala430Val(p.A430V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355962
Start 71572309:71572309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.583G>A
AA Mutation p.Glu195Lys(p.E195K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355962
Start 71576406:71576406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10T>C
AA Mutation p.Tyr4His(p.Y4H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355962
Start 71572269:71572269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623A>C
AA Mutation p.Lys208Thr(p.K208T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000355962
Start 71576300:71576300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.116C>A
AA Mutation p.Ala39Asp(p.A39D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000355962
Start 71568216:71568216(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1293C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000355962
Start 71571627:71571627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.738T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000355962
Start 71572298:71572298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.594G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000355962
Start 71576019:71576019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.243T>C
Mutation Classification Silent
Feature Type Transcript