Primary Site >> Liver Cancer

Gene >> SETD1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000604567
Start 121814890:121814890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2675C>T
AA Mutation p.Ala892Val(p.A892V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000604567
Start 121809694:121809694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.749C>A
AA Mutation p.Thr250Lys(p.T250K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000604567
Start 121823249:121823249(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4670A>T
AA Mutation p.Gln1557Leu(p.Q1557L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000604567
Start 121809977:121809977(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs547856709
CDS Mutation c.1032C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000604567
Start 121827566:121827566(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5385G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000604567
Start 121823424:121823424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4845C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000604567
Start 121809995:121809995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1050G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000604567
Start 121822593:121822593(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4014G>T
Mutation Classification Silent
Feature Type Transcript