Annotation Detail

Information
Associated Genes
LIG4
Associated Variants
LIG4 p.Thr9Ile (p.T9I) ( ENST00000687164.1, ENST00000688595.1, ENST00000686204.1, ENST00000688396.1, ENST00000686095.1, ENST00000685338.1, ENST00000686913.1, ENST00000689762.1, ENST00000614526.2, ENST00000611712.4, ENST00000687822.1, ENST00000405925.2, ENST00000693040.1, ENST00000686926.1, ENST00000692222.1, ENST00000688529.1, ENST00000442234.6, ENST00000690127.1, ENST00000688455.1 )
LIG4 p.Thr9Ile (p.T9I) ( ENST00000405925.2, ENST00000442234.6, ENST00000611712.4, ENST00000614526.2, ENST00000685338.1, ENST00000686095.1, ENST00000686204.1, ENST00000686913.1, ENST00000686926.1, ENST00000687164.1, ENST00000687822.1, ENST00000688396.1, ENST00000688455.1, ENST00000688529.1, ENST00000688595.1, ENST00000689762.1, ENST00000690127.1, ENST00000692222.1, ENST00000693040.1 )
Associated Disease
Multiple myeloma, resistance to
Source Database
ClinVar
Description
NM_206937.2(LIG4):c.26C>T (p.Thr9Ile) AND Multiple myeloma, resistance to
ClinVar Allele ID
22716
ClinVar RefSeq Alternation Syntax
NM_001352598.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_002312.3:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001379095.1:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001352599.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001352601.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001352604.2:c.89-27C>T
ClinVar RefSeq Alternation Syntax
NM_001352600.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001352602.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001352603.1:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_001330595.2:c.-149-27C>T
ClinVar RefSeq Alternation Syntax
NM_001098268.2:c.26C>T
ClinVar RefSeq Alternation Syntax
NM_206937.2:c.26C>T
Clinical Significance Description
protective
Clinical Significance Last Update
2015-05-18
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000008116
ClinVar Disease
Multiple myeloma, resistance to
Observed Origin Sample
germline
Pubmed
12471202
Drugs