Primary Site >> Liver Cancer

Gene >> ADAMTS7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78766903:78766903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3008C>A
AA Mutation p.Pro1003His(p.P1003H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78774758:78774758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1742G>T
AA Mutation p.Arg581Leu(p.R581L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78764089:78764089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4430G>C
AA Mutation p.Ser1477Thr(p.S1477T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78766133:78766133(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3778C>A
AA Mutation p.Leu1260Met(p.L1260M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78774653:78774653(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1847T>A
AA Mutation p.Leu616Gln(p.L616Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000388820
Start 78771242:78771242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2438G>A
AA Mutation p.Gly813Asp(p.G813D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000388820
Start 78800219:78800219(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.429G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000388820
Start 78798027:78798027(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.543T>C
Mutation Classification Silent
Feature Type Transcript