Primary Site >> Stomach Cancer

Gene >> MLKL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308807
Start 74675089:74675089(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372403777
CDS Mutation c.1252G>A
AA Mutation p.Glu418Lys(p.E418K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308807
Start 74682744:74682744(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863T>G
AA Mutation p.Leu288Arg(p.L288R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308807
Start 74695657:74695657(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747075913
CDS Mutation c.101G>A
AA Mutation p.Arg34His(p.R34H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308807
Start 74695396:74695396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764970932
CDS Mutation c.362G>A
AA Mutation p.Arg121His(p.R121H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000308807
Start 74695401:74695401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000308807
Start 74695307:74695307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000308807
Start 74691416:74691416(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.583G>T
AA Mutation p.Glu195Ter(p.E195*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript