Primary Site >> Liver Cancer

Gene >> KIAA1109

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122264296:122264296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7186A>C
AA Mutation p.Asn2396His(p.N2396H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122339357:122339357(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12301A>G
AA Mutation p.Asn4101Asp(p.N4101D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122346661:122346661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12772A>G
AA Mutation p.Met4258Val(p.M4258V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122263535:122263535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7076G>A
AA Mutation p.Gly2359Asp(p.G2359D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122347731:122347731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13081G>C
AA Mutation p.Ala4361Pro(p.A4361P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122272180:122272180(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8221C>G
AA Mutation p.Pro2741Ala(p.P2741A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122315582:122315582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10433T>A
AA Mutation p.Leu3478Gln(p.L3478Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122207238:122207238(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764953885
CDS Mutation c.1627G>A
AA Mutation p.Asp543Asn(p.D543N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122353939:122353939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767116983
CDS Mutation c.14227C>T
AA Mutation p.Arg4743Cys(p.R4743C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122258838:122258838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6757A>G
AA Mutation p.Ile2253Val(p.I2253V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122352939:122352939(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13885G>A
AA Mutation p.Val4629Ile(p.V4629I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122201064:122201064(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1436G>T
AA Mutation p.Cys479Phe(p.C479F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264501
Start 122244022:122244022(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4911A>T
AA Mutation p.Leu1637Phe(p.L1637F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000264501
Start 122347616:122347616(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12966G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000264501
Start 122258828:122258828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6747T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000264501
Start 122316858:122316858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10666C>T
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000264501
Start 122325278:122325278(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10953A>T
Mutation Classification Silent
Feature Type Transcript