Primary Site >> Stomach Cancer

Gene >> GHR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42695041:42695041(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.391A>G
AA Mutation p.Ser131Gly(p.S131G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42699914:42699914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.530C>A
AA Mutation p.Ala177Glu(p.A177E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42718468:42718468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.961G>A
AA Mutation p.Glu321Lys(p.E321K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42719279:42719279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1772C>T
AA Mutation p.Pro591Leu(p.P591L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42629050:42629050(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.83T>A
AA Mutation p.Ile28Asn(p.I28N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42719402:42719402(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1895A>C
AA Mutation p.Gln632Pro(p.Q632P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42718772:42718772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1265A>G
AA Mutation p.Asp422Gly(p.D422G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42689001:42689001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248A>G
AA Mutation p.Gln83Arg(p.Q83R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000230882
Start 42719048:42719048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1541G>A
AA Mutation p.Cys514Tyr(p.C514Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000230882
Start 42719031:42719031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1524G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000230882
Start 42719304:42719304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1797T>C
Mutation Classification Silent
Feature Type Transcript