ClinVar Miner

List of variants in gene KL reported as benign for not provided

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_004795.4(KL):c.2619T>C (p.Asn873=) rs649964 0.97241
NM_004795.4(KL):c.273T>C (p.Asp91=) rs2772364 0.94529
NC_000013.11:g.33016276G>A rs2516569 0.91192
NM_004795.4(KL):c.2701+22T>A rs650439 0.81086
NM_004795.4(KL):c.2247T>C (p.Ala749=) rs648202 0.76534
NM_004795.4(KL):c.1331-195A>G rs2149860 0.43117
NM_004795.4(KL):c.1767C>T (p.His589=) rs564481 0.30857
NM_004795.4(KL):c.820-144A>G rs7323281 0.26050
NM_004795.4(KL):c.1109G>C (p.Cys370Ser) rs9527025 0.15805
NM_004795.4(KL):c.820-211G>A rs9527024 0.15800
NM_004795.4(KL):c.1155G>A (p.Lys385=) rs9527026 0.15795
NM_004795.4(KL):c.1330+143T>G rs7997728 0.15793
NM_004795.4(KL):c.820-79C>T rs9536312 0.15790
NM_004795.4(KL):c.820-46C>G rs9536313 0.15788
NM_004795.4(KL):c.1054T>G (p.Phe352Val) rs9536314 0.15781
NM_004795.4(KL):c.1599+205C>T rs9527029 0.06147
NM_004795.4(KL):c.1593C>T (p.Tyr531=) rs62637617 0.03076
NM_004795.4(KL):c.2702-110T>C rs59355325 0.02365
NM_004795.4(KL):c.2702-182C>T rs7330273 0.02156
NM_004795.4(KL):c.1540C>T (p.Pro514Ser) rs3752472 0.01461
NM_004795.4(KL):c.1407T>C (p.Gly469=) rs138916294 0.01262
NM_004795.4(KL):c.140G>A (p.Arg47Gln) rs201936594 0.01179
NM_004795.4(KL):c.595C>T (p.Arg199Cys) rs200063460 0.00849
NM_004795.4(KL):c.326T>G (p.Leu109Arg) rs35239775 0.00735
NM_004795.4(KL):c.320C>T (p.Ala107Val) rs115511178 0.00702
NM_004795.4(KL):c.87C>T (p.Arg29=) rs528826951 0.00696
NM_004795.4(KL):c.607G>T (p.Ala203Ser) rs116289670 0.00657
NM_004795.4(KL):c.3008A>G (p.Tyr1003Cys) rs35328951 0.00553
NM_004795.4(KL):c.393C>A (p.Asn131Lys) rs79554512 0.00458
NM_004795.4(KL):c.327G>C (p.Leu109=) rs116810451 0.00457
NM_004795.4(KL):c.91C>T (p.Leu31=) rs540806300 0.00421
NM_004795.4(KL):c.1331-39G>A rs199758453 0.00255
NM_004795.4(KL):c.1371A>C (p.Ala457=) rs150268586 0.00202
NM_004795.4(KL):c.2626G>A (p.Asp876Asn) rs146235320 0.00193
NM_004795.4(KL):c.2532G>A (p.Gln844=) rs149775738 0.00111
NM_004795.4(KL):c.1965C>T (p.Gly655=) rs144345203 0.00098
NM_004795.4(KL):c.2688C>T (p.Asn896=) rs145682430 0.00067
NM_004795.4(KL):c.639C>A (p.Ala213=) rs387907445 0.00067
NM_004795.4(KL):c.537G>C (p.Arg179=) rs769292412 0.00060
NM_004795.4(KL):c.1188A>G (p.Gln396=) rs139912465 0.00053
NM_004795.4(KL):c.387C>T (p.Tyr129=) rs373385333 0.00021
NM_004795.4(KL):c.450C>A (p.Ser150=) rs764992732 0.00011
NM_004795.4(KL):c.2259G>A (p.Leu753=) rs200040161 0.00008
NM_004795.4(KL):c.747C>T (p.Ala249=) rs563017227 0.00007
NM_004795.4(KL):c.486G>A (p.Ala162=) rs371131557 0.00001
NM_004795.4(KL):c.1330+11G>A
NM_004795.4(KL):c.2296G>A (p.Gly766Ser) rs114752661
NM_004795.4(KL):c.2702-59dup rs34137141
NM_004795.4(KL):c.820-236C>T rs9536311
NM_004795.4(KL):c.820-75T>G rs570875

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