Primary Site >> Stomach Cancer

Gene >> SLC12A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262461
Start 128184792:128184792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs116065946
CDS Mutation c.3439T>C
AA Mutation p.Tyr1147His(p.Y1147H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262461
Start 128112853:128112853(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.796A>G
AA Mutation p.Thr266Ala(p.T266A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262461
Start 128147635:128147635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1787T>C
AA Mutation p.Val596Ala(p.V596A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262461
Start 128174618:128174618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2881G>T
AA Mutation p.Asp961Tyr(p.D961Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262461
Start 128186620:128186620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3628T>G
AA Mutation p.Phe1210Val(p.F1210V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262461
Start 128184378:128184378(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3312T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262461
Start 128151311:128151311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2178A>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000262461
Start 128084534:128084534(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.582delG
AA Mutation p.His195ThrfsTer89(p.H195Tfs*89)
Mutation Classification Frame_Shift_Del
Feature Type Transcript