Primary Site >> Stomach Cancer

Gene >> HLF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000226067
Start 55320743:55320743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.752A>G
AA Mutation p.Asn251Ser(p.N251S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000226067
Start 55320719:55320719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.728G>A
AA Mutation p.Arg243His(p.R243H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000226067
Start 55315419:55315419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.644G>A
AA Mutation p.Arg215His(p.R215H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000226067
Start 55320782:55320782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.791A>G
AA Mutation p.Asn264Ser(p.N264S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000226067
Start 55315255:55315255(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.480A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000226067
Start 55265532:55265532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.48G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000226067
Start 55267927:55267927(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.297delC
AA Mutation p.Ser100AlafsTer106(p.S100Afs*106)
Mutation Classification Frame_Shift_Del
Feature Type Transcript