Primary Site >> Liver Cancer

Gene >> DMBT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122618197:122618197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4685C>A
AA Mutation p.Ala1562Asp(p.A1562D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122631105:122631105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5783G>C
AA Mutation p.Gly1928Ala(p.G1928A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122643280:122643280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7124A>G
AA Mutation p.Tyr2375Cys(p.Y2375C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122592560:122592560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2465G>C
AA Mutation p.Cys822Ser(p.C822S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122576424:122576424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.309G>T
AA Mutation p.Arg103Ser(p.R103S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122576702:122576702(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.587A>G
AA Mutation p.Asp196Gly(p.D196G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122599014:122599014(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3197A>G
AA Mutation p.Glu1066Gly(p.E1066G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122570204:122570204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.134C>T
AA Mutation p.Ala45Val(p.A45V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000338354
Start 122601931:122601931(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3478T>C
AA Mutation p.Cys1160Arg(p.C1160R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000338354
Start 122576430:122576430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.315G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000338354
Start 122602089:122602089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3636C>T
Mutation Classification Silent
Feature Type Transcript