Primary Site >> Liver Cancer

Gene >> EIF2AK4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 40029420:40029420(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754527586
CDS Mutation c.4517A>G
AA Mutation p.Asn1506Ser(p.N1506S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 40020964:40020964(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4239C>G
AA Mutation p.Ile1413Met(p.I1413M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 39949160:39949160(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.405C>A
AA Mutation p.Ser135Arg(p.S135R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 39976448:39976448(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1853T>C
AA Mutation p.Val618Ala(p.V618A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 39972936:39972936(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1582T>G
AA Mutation p.Trp528Gly(p.W528G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 39972937:39972937(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1583G>T
AA Mutation p.Trp528Leu(p.W528L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 40020995:40020995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4270A>G
AA Mutation p.Ile1424Val(p.I1424V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263791
Start 39967426:39967426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1100A>G
AA Mutation p.Lys367Arg(p.K367R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263791
Start 39976440:39976440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1845C>T
Mutation Classification Silent
Feature Type Transcript