Primary Site >> Stomach Cancer

Gene >> PTN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000348225
Start 137253541:137253541(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.212G>A
AA Mutation p.Arg71Gln(p.R71Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000348225
Start 137253622:137253622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.131A>C
AA Mutation p.Lys44Thr(p.K44T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000348225
Start 137253586:137253586(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167T>C
AA Mutation p.Val56Ala(p.V56A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000348225
Start 137251256:137251256(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.425G>A
AA Mutation p.Gly142Asp(p.G142D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000348225
Start 137254926:137254926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.48C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000348225
Start 137251288:137251288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.393C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000348225
Start 137253630:137253630(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.123delA
AA Mutation p.Val42Ter(p.V42*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript