Primary Site >> Liver Cancer

Gene >> ADAMTS9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64654407:64654407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1262G>A
AA Mutation p.Ser421Asn(p.S421N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64647968:64647968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1682C>A
AA Mutation p.Ala561Asp(p.A561D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64631865:64631865(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2236G>C
AA Mutation p.Gly746Arg(p.G746R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64541154:64541154(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5462C>A
AA Mutation p.Ala1821Asp(p.A1821D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64613419:64613419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3280G>C
AA Mutation p.Glu1094Gln(p.E1094Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64602026:64602026(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3935A>G
AA Mutation p.Glu1312Gly(p.E1312G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64681314:64681314(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.566A>T
AA Mutation p.Gln189Leu(p.Q189L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000498707
Start 64648008:64648008(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1642G>C
AA Mutation p.Gly548Arg(p.G548R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000498707
Start 64596980:64596980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4029C>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000498707
Start 64622450:64622450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2526A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000498707
Start 64596887:64596887(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4122G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000498707
Start 64594280:64594280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4334G>A
AA Mutation p.Trp1445Ter(p.W1445*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript