Primary Site >> Liver Cancer

Gene >> CR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207474971:207474971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2294A>T
AA Mutation p.Asp765Val(p.D765V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207476275:207476275(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2581A>C
AA Mutation p.Asn861His(p.N861H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207476285:207476285(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2591G>A
AA Mutation p.Gly864Asp(p.G864D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207473836:207473836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2014C>T
AA Mutation p.Leu672Phe(p.L672F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207469937:207469937(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1060C>A
AA Mutation p.Pro354Thr(p.P354T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207470868:207470868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1354C>G
AA Mutation p.Gln452Glu(p.Q452E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207473814:207473814(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1992T>A
AA Mutation p.His664Gln(p.H664Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207470746:207470746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1232A>G
AA Mutation p.Gln411Arg(p.Q411R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207476416:207476416(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2722A>G
AA Mutation p.Lys908Glu(p.K908E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000367058
Start 207471017:207471017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1423G>A
AA Mutation p.Gly475Arg(p.G475R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000367058
Start 207476274:207476274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2580G>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000367058
Start 207477973:207477973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2814T>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000367058
Start 207468561:207468561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.480C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000367058
Start 207472788:207472788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1587A>T
Mutation Classification Silent
Feature Type Transcript