Primary Site >> Stomach Cancer

Gene >> HRH2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175684275:175684275(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1042A>G
AA Mutation p.Thr348Ala(p.T348A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175683588:175683588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355G>A
AA Mutation p.Ala119Thr(p.A119T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175683613:175683613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.380C>A
AA Mutation p.Pro127His(p.P127H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175683582:175683582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.349T>C
AA Mutation p.Tyr117His(p.Y117H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175683460:175683460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.227C>A
AA Mutation p.Ala76Asp(p.A76D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000231683
Start 175683883:175683883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.650A>G
AA Mutation p.Asn217Ser(p.N217S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000231683
Start 175684229:175684229(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996C>A
Mutation Classification Silent
Feature Type Transcript