Primary Site >> Liver Cancer

Gene >> SUSD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358321
Start 24187397:24187397(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1838G>T
AA Mutation p.Arg613Leu(p.R613L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358321
Start 24185782:24185782(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758581195
CDS Mutation c.1192C>T
AA Mutation p.Arg398Cys(p.R398C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358321
Start 24188287:24188287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2404G>A
AA Mutation p.Ala802Thr(p.A802T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000358321
Start 24185209:24185209(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.898G>A
AA Mutation p.Glu300Lys(p.E300K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000358321
Start 24187235:24187235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1676T>C
AA Mutation p.Val559Ala(p.V559A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000358321
Start 24186086:24186086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1410G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000358321
Start 24187451:24187451(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1891+1G>C
Mutation Classification Splice_Site
Feature Type Transcript