Primary Site >> Stomach Cancer

Gene >> NKX2-2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377142
Start 21512249:21512249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.496C>T
AA Mutation p.Arg166Cys(p.R166C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377142
Start 21512332:21512332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413C>T
AA Mutation p.Ala138Val(p.A138V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377142
Start 21512096:21512096(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763629654
CDS Mutation c.649G>A
AA Mutation p.Ala217Thr(p.A217T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377142
Start 21512030:21512030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.715G>A
AA Mutation p.Ala239Thr(p.A239T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000377142
Start 21513574:21513574(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372356384
CDS Mutation c.96G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000377142
Start 21512097:21512097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.648C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000377142
Start 21512469:21512469(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.276C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000377142
Start 21513634:21513634(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.36C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000377142
Start 21512055:21512055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.690G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000377142
Start 21511973:21511973(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.772delC
AA Mutation p.Gln258SerfsTer59(p.Q258Sfs*59)
Mutation Classification Frame_Shift_Del
Feature Type Transcript