Primary Site >> Stomach Cancer

Gene >> TELO2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1500473:1500473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200293618
CDS Mutation c.1129C>T
AA Mutation p.Arg377Trp(p.R377W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1495567:1495567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.557G>A
AA Mutation p.Arg186His(p.R186H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1501486:1501486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1348G>A
AA Mutation p.Ala450Thr(p.A450T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1506319:1506319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780227352
CDS Mutation c.2116C>T
AA Mutation p.Arg706Cys(p.R706C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1494533:1494533(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252G>T
AA Mutation p.Glu84Asp(p.E84D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1506292:1506292(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145891685
CDS Mutation c.2089G>A
AA Mutation p.Gly697Ser(p.G697S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1494427:1494427(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.146G>A
AA Mutation p.Arg49Lys(p.R49K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1501730:1501730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs572277163
CDS Mutation c.1429G>A
AA Mutation p.Val477Ile(p.V477I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262319
Start 1506269:1506269(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2066C>T
AA Mutation p.Pro689Leu(p.P689L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262319
Start 1502758:1502758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1767C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000262319
Start 1502704:1502704(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1713A>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000262319
Start 1506267:1506267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2064C>T
Mutation Classification Silent
Feature Type Transcript