List of variants in gene combination BRCA2, LOC106721785 reported as uncertain significance

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 48

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.-41G>A	rs879255312	0.00004
NM_000059.4(BRCA2):c.-143C>T	rs1453200112	0.00001
NM_000059.4(BRCA2):c.-40+4A>G	rs1429193506	0.00001
NM_000059.4(BRCA2):c.-40+5G>T	rs930825419	0.00001
NM_000059.4(BRCA2):c.-40+7G>T	rs1555279969	0.00001
NM_000059.4(BRCA2):c.-88G>T	rs917232759	0.00001
NC_000013.11:g.(?_32315480)_(32315687_?)del
NC_000013.11:g.32315397C>T
NC_000013.11:g.32315482_32316529dup
NM_000059.3(BRCA2):c.-210A>G	rs886050111
NM_000059.3(BRCA2):c.-220G>T	rs1036870835
NM_000059.4(BRCA2):c.-125G>C
NM_000059.4(BRCA2):c.-143_-142insCGTCTTTTAGCATACAGGTCTTGTGCAGCTTTTATCAGATTTCTTCCTCTAAGTCTTGATACTTTTTTTTTTTTTAATAATACTTTAAGTTCCGCAATACATGTGCAGAACCTGCAGGTTTGTTACATAGGTATACACGTGCCATGGTGGTTTGCTACACCCATCAACCTGTCATCTACATTAGATATTTCTCCTAATGCTATCCCTTCCCTAGCCCCCCATCCCCCAATAGCCCCCGGTGTGTGATGTTCCCTGCCCTGTGTCCACGTGTTCTCATTGTTCAACTCCCACTTATCAGTGAGAACACGCGGTGTTTGTTTTTCTGTTCTCGTGTTATTTTTCTGAGAATGATATGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATTCTTTTTTATGGCCACATAGTATTCTGTGGTGTATATGGGCCACATTTTCTTTATCCAGTCTATCATTGATGGGCATTTGGGTAGGTTCCAAGTCTTTGCTAATTTTGAAATTATCATTTCACAGCTTAATTTCTGATGGTTCCTTGCTAGTATTTAGAAATACAATTGATTTTTTTATGTTGATCTTAAAAAATTGCAAGCTTACCTATCTTGTTTATTAGATCTAGTAACTTATTTGTAGATTCCATTGGGTTTTCTACAAATAGACTCATGTTGCCTAAGAATAAAGGCTTACTTTTTTCCCACTATGAATCCTTTTTATTTGTATTTTTTTCCTTGCCTTATTGCACTGGCTAGAATCTAAAGTATAATGTTGAACAGACATGGTGAGAGCAGATATTCTTACAACTGACCCACACTTAGGTTTGTGGAGAAAGCACTCAGTCTTTCACCATTAAGTATGTTAACTGTACTTAGTTAACTGTAGGGC
NM_000059.4(BRCA2):c.-152T>C
NM_000059.4(BRCA2):c.-179_-169dup	rs1484668823
NM_000059.4(BRCA2):c.-188C>T	rs556172218
NM_000059.4(BRCA2):c.-196G>A	rs1555279932
NM_000059.4(BRCA2):c.-40+10_-40+15del
NM_000059.4(BRCA2):c.-40+15T>C
NM_000059.4(BRCA2):c.-40+17G>C
NM_000059.4(BRCA2):c.-40+1G>A	rs2072249096
NM_000059.4(BRCA2):c.-40+1G>C	rs2072249096
NM_000059.4(BRCA2):c.-40+1G>T
NM_000059.4(BRCA2):c.-40+2T>A
NM_000059.4(BRCA2):c.-40+2T>C	rs1593879845
NM_000059.4(BRCA2):c.-40+4_-40+6del
NM_000059.4(BRCA2):c.-40+5G>C
NM_000059.4(BRCA2):c.-40+6T>A	rs2138695750
NM_000059.4(BRCA2):c.-40G>A	rs1555279967
NM_000059.4(BRCA2):c.-40G>C	rs1555279967
NM_000059.4(BRCA2):c.-40G>T	rs1555279967
NM_000059.4(BRCA2):c.-41_-40+5del	rs2138695709
NM_000059.4(BRCA2):c.-42C>T	rs536354307
NM_000059.4(BRCA2):c.-43G>A	rs2138695686
NM_000059.4(BRCA2):c.-43G>T
NM_000059.4(BRCA2):c.-45G>T
NM_000059.4(BRCA2):c.-48C>G
NM_000059.4(BRCA2):c.-48C>T
NM_000059.4(BRCA2):c.-51C>T	rs1057521841
NM_000059.4(BRCA2):c.-52A>C
NM_000059.4(BRCA2):c.-53C>T	rs2072248746
NM_000059.4(BRCA2):c.-54G>A	rs1209443446
NM_000059.4(BRCA2):c.-56C>A	rs1555279958
NM_000059.4(BRCA2):c.-57A>G	rs1593879801
NM_000059.4(BRCA2):c.-59G>C
NM_000059.4(BRCA2):c.-59_-57del	rs545321666
NM_000059.4(BRCA2):c.-60A>G	rs1057522793
NM_000059.4(BRCA2):c.-60A>T

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