ClinVar Miner

List of variants in gene BMPER reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001365308.1(BMPER):c.408C>T (p.Gly136=) rs10265207 0.42558
NM_001365308.1(BMPER):c.*1217A>G rs2058681 0.25122
NM_001365308.1(BMPER):c.1461G>T (p.Pro487=) rs77064045 0.24267
NM_001365308.1(BMPER):c.*1067C>T rs17169667 0.23581
NM_001365308.1(BMPER):c.*704A>G rs11972404 0.09741
NM_001365308.1(BMPER):c.*1262C>T rs60064022 0.09316
NM_001365308.1(BMPER):c.*2218C>T rs73097004 0.09281
NM_001365308.1(BMPER):c.*1703C>T rs73097003 0.08312
NM_133468.5(BMPER):c.-141+4A>G rs113711026 0.02814
NM_001365308.1(BMPER):c.474G>A (p.Met158Ile) rs62623441 0.02800
NM_133468.5(BMPER):c.-211G>A rs112890951 0.02724
NM_001365308.1(BMPER):c.133+9G>C rs75250304 0.01271
NM_133468.5(BMPER):c.-230G>A rs189473686 0.01178
NM_001365308.1(BMPER):c.-25C>A rs75295552 0.01000
NM_001365308.1(BMPER):c.774T>G (p.Ala258=) rs117988035 0.00895
NM_001365308.1(BMPER):c.580G>A (p.Gly194Ser) rs74734392 0.00867
NM_001365308.1(BMPER):c.1086C>T (p.Gly362=) rs116085783 0.00804
NM_133468.5(BMPER):c.-263G>A rs117405942 0.00523
NM_001365308.1(BMPER):c.*11G>A rs142523304 0.00498
NM_001365308.1(BMPER):c.1087G>A (p.Val363Ile) rs117322489 0.00405
NM_001365308.1(BMPER):c.*522G>A rs118049461 0.00250
NM_001365308.1(BMPER):c.*278T>C rs116981158 0.00103
NM_001365308.1(BMPER):c.*384T>G rs536841746 0.00002
NM_001365308.1(BMPER):c.*126TA[7] rs68052795
NM_001365308.1(BMPER):c.*678G>T rs77835415
NM_001365308.1(BMPER):c.1935G>C (p.Thr645=) rs6968741
NM_133468.5(BMPER):c.-313G>C rs114417992

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