Primary Site >> Stomach Cancer

Gene >> POMT2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77279898:77279898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201117837
CDS Mutation c.1816G>A
AA Mutation p.Ala606Thr(p.A606T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77301235:77301235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.671C>T
AA Mutation p.Pro224Leu(p.P224L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77280046:77280046(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1760T>C
AA Mutation p.Phe587Ser(p.F587S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77311975:77311975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.307T>C
AA Mutation p.Phe103Leu(p.F103L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77278782:77278782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1979T>C
AA Mutation p.Val660Ala(p.V660A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261534
Start 77278785:77278785(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770606360
CDS Mutation c.1976G>A
AA Mutation p.Arg659Gln(p.R659Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261534
Start 77278826:77278826(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141193672
CDS Mutation c.1935C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261534
Start 77280398:77280398(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1719C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000261534
Start 77284963:77284963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1563T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000261534
Start 77285005:77285005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1521C>T
Mutation Classification Silent
Feature Type Transcript