Primary Site >> Liver Cancer

Gene >> ADAM23

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264377
Start 206565040:206565040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1366T>A
AA Mutation p.Trp456Arg(p.W456R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264377
Start 206573139:206573139(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1681C>T
AA Mutation p.Arg561Trp(p.R561W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264377
Start 206573160:206573160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1702G>C
AA Mutation p.Asp568His(p.D568H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264377
Start 206560026:206560026(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1077T>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264377
Start 206571771:206571771(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1611G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence splice_donor_variant
Transcription ID ENST00000264377
Start 206481310:206481310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.509+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264377
Start 206571725:206571725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1567-2A>T
Mutation Classification Splice_Site
Feature Type Transcript