ClinVar Miner

List of variants in gene LDLRAP1 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_015627.3(LDLRAP1):c.653C>T (p.Thr218Ile) rs114583297 0.00817
NM_015627.3(LDLRAP1):c.672C>T (p.Ser224=) rs41291054 0.00191
NM_015627.3(LDLRAP1):c.*478C>T rs370958045 0.00164
NM_015627.3(LDLRAP1):c.*430G>T rs186747548 0.00135
NM_015627.3(LDLRAP1):c.*1395C>G rs573882275 0.00084
NM_015627.3(LDLRAP1):c.284G>A (p.Arg95Gln) rs139877665 0.00061
NM_015627.3(LDLRAP1):c.*1677G>A rs528624038 0.00056
NM_015627.3(LDLRAP1):c.396C>T (p.Ile132=) rs369497122 0.00054
NM_015627.3(LDLRAP1):c.*810C>T rs111431438 0.00041
NM_015627.3(LDLRAP1):c.*1824T>C rs775249141 0.00033
NM_015627.3(LDLRAP1):c.451C>T (p.Arg151Trp) rs148916767 0.00032
NM_015627.3(LDLRAP1):c.*961A>G rs375492783 0.00024
NM_015627.3(LDLRAP1):c.907G>A (p.Asp303Asn) rs199605881 0.00024
NM_015627.3(LDLRAP1):c.375C>T (p.His125=) rs146134293 0.00015
NM_015627.3(LDLRAP1):c.*1032G>A rs879931315 0.00014
NM_015627.3(LDLRAP1):c.622G>A (p.Ala208Thr) rs146122441 0.00012
NM_015627.3(LDLRAP1):c.*1201G>A rs1055321575 0.00011
NM_015627.3(LDLRAP1):c.*1515C>T rs72662610 0.00010
NM_015627.3(LDLRAP1):c.423C>T (p.Leu141=) rs140170877 0.00010
NM_015627.3(LDLRAP1):c.*535C>T rs1057515493 0.00006
NM_015627.3(LDLRAP1):c.*877C>T rs1057515465 0.00006
NM_015627.3(LDLRAP1):c.747+13G>A rs202247605 0.00006
NM_015627.3(LDLRAP1):c.201G>A (p.Ser67=) rs747011377 0.00005
NM_015627.3(LDLRAP1):c.*1737G>A rs1038619262 0.00003
NM_015627.3(LDLRAP1):c.*435A>G rs1448105558 0.00003
NM_015627.3(LDLRAP1):c.*1430C>T rs1057515430 0.00002
NM_015627.3(LDLRAP1):c.*28G>A rs140712823 0.00002
NM_015627.3(LDLRAP1):c.*717C>T rs888167861 0.00002
NM_015627.3(LDLRAP1):c.*821T>G rs1057515494 0.00002
NM_015627.3(LDLRAP1):c.*1040A>C rs531672783 0.00001
NM_015627.3(LDLRAP1):c.*1233C>T rs942302853 0.00001
NM_015627.3(LDLRAP1):c.*1284C>T rs1057515429 0.00001
NM_015627.3(LDLRAP1):c.*1375C>T rs574638156 0.00001
NM_015627.3(LDLRAP1):c.*1477T>G rs1057515540 0.00001
NM_015627.3(LDLRAP1):c.*1556A>C rs1057515496 0.00001
NM_015627.3(LDLRAP1):c.*259C>A rs767635119 0.00001
NM_015627.3(LDLRAP1):c.*614T>C rs1009323668 0.00001
NM_015627.3(LDLRAP1):c.*804G>A rs1057515464 0.00001
NM_015627.3(LDLRAP1):c.*868C>G rs1057515495 0.00001
NM_015627.3(LDLRAP1):c.771A>C (p.Glu257Asp) rs2044445441 0.00001
NM_015627.3(LDLRAP1):c.*1682C>A rs763698849
NM_015627.3(LDLRAP1):c.*1718del rs544756299
NM_015627.3(LDLRAP1):c.*253G>A rs929775060
NM_015627.3(LDLRAP1):c.*331C>T rs1057515426
NM_015627.3(LDLRAP1):c.*607G>T rs1057515427
NM_015627.3(LDLRAP1):c.*63G>T rs62619761
NM_015627.3(LDLRAP1):c.*814G>A rs1057515428
NM_015627.3(LDLRAP1):c.*941G>T rs2044527626
NM_015627.3(LDLRAP1):c.276G>A (p.Val92=) rs1215026981
NM_015627.3(LDLRAP1):c.414C>T (p.Asn138=) rs1057515536
NM_015627.3(LDLRAP1):c.480C>T (p.Thr160=) rs1057515463
NM_015627.3(LDLRAP1):c.487C>T (p.Gln163Ter) rs1057515537

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