Primary Site >> Stomach Cancer

Gene >> PTHLH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395872
Start 27963591:27963591(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.281G>A
AA Mutation p.Arg94Gln(p.R94Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395872
Start 27963679:27963679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.193G>A
AA Mutation p.Ala65Thr(p.A65T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000395872
Start 27969459:27969459(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377444886
CDS Mutation c.36G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000395872
Start 27963644:27963644(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745833158
CDS Mutation c.228G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000395872
Start 27963466:27963466(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.406C>T
AA Mutation p.Gln136Ter(p.Q136*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript