Primary Site >> Liver Cancer

Gene >> ASH1L

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155480670:155480670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2200C>A
AA Mutation p.Leu734Ile(p.L734I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155342021:155342021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8390T>G
AA Mutation p.Ile2797Ser(p.I2797S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155478323:155478323(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4547G>C
AA Mutation p.Arg1516Pro(p.R1516P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155438408:155438408(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5747G>T
AA Mutation p.Arg1916Ile(p.R1916I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000368346
Start 155349596:155349596(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7382A>G
AA Mutation p.Asp2461Gly(p.D2461G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155481668:155481668(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1202A>T
AA Mutation p.Asn401Ile(p.N401I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155479278:155479278(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3592C>A
AA Mutation p.Pro1198Thr(p.P1198T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368346
Start 155338280:155338280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8627A>C
AA Mutation p.Asn2876Thr(p.N2876T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000368346
Start 155481232:155481232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1638A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000368346
Start 155480512:155480512(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2358A>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000368346
Start 155479495:155479495(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3375A>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000368346
Start 155478385:155478385(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4485delT
AA Mutation p.Glu1496AsnfsTer19(p.E1496Nfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000368346
Start 155480139:155480140(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2721_2730dupACTGTCAGTG
AA Mutation p.Ala911ThrfsTer10(p.A911Tfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript