ClinVar Miner

List of variants in gene PRDM16 reported as benign for not provided

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_022114.4(PRDM16):c.677-294A>G rs1889124 0.79518
NM_022114.4(PRDM16):c.884+112C>T rs12562397 0.56835
NM_022114.4(PRDM16):c.884+119C>G rs12562399 0.55696
NM_022114.4(PRDM16):c.3110-85G>A rs2244013 0.39045
NM_022114.4(PRDM16):c.3522-262G>C rs2493274 0.37921
NM_022114.4(PRDM16):c.3697-107T>C rs10752734 0.35672
NM_022114.4(PRDM16):c.574-141T>G rs871822 0.34081
NM_022114.4(PRDM16):c.676+125G>A rs7535965 0.33448
NM_022114.4(PRDM16):c.884+215G>A rs4471209 0.24840
NM_022114.4(PRDM16):c.3697-146_3697-139del rs879837688 0.20438
NM_022114.4(PRDM16):c.885-169G>A rs3795261 0.16738
NM_022114.4(PRDM16):c.3284+145A>G rs870170 0.16090
NM_022114.4(PRDM16):c.574-92C>T rs12726710 0.15840
NM_022114.4(PRDM16):c.2604-240G>A rs2493288 0.15167
NM_022114.4(PRDM16):c.3697-137_3697-68del rs1557674947 0.13296
NM_022114.4(PRDM16):c.3697-68T>C rs2493271 0.11383
NM_022114.4(PRDM16):c.3284+179G>A rs75861985 0.10946
NM_022114.4(PRDM16):c.677-111G>A rs78946683 0.10941
NM_022114.4(PRDM16):c.884+245C>T rs2493306 0.09240
NM_022114.4(PRDM16):c.*50A>G rs2493270 0.09233
NM_022114.4(PRDM16):c.2604-237C>T rs56353807 0.08738
NM_022114.4(PRDM16):c.3109+50C>T rs11805974 0.06994
NM_022114.4(PRDM16):c.1033-76G>A rs2493305 0.06831
NM_022114.4(PRDM16):c.3697-276G>A rs2483247 0.06119
NM_022114.4(PRDM16):c.3285-81A>G rs2493276 0.05950
NM_022114.4(PRDM16):c.3697-137_3697-107del rs1557674940 0.05893
NM_022114.4(PRDM16):c.1186+171G>A rs79350670 0.05007
NM_022114.4(PRDM16):c.885-136C>A rs41315264 0.04799
NM_022114.4(PRDM16):c.2604-128G>A rs76153297 0.04505
NM_022114.4(PRDM16):c.1187-143C>T rs57382922 0.04359
NM_022114.4(PRDM16):c.2939+91G>T rs114150379 0.04262
NM_022114.4(PRDM16):c.2603+217G>A rs72633334 0.04131
NM_022114.4(PRDM16):c.3697-146T>C rs28551116 0.04084
NM_022114.4(PRDM16):c.1186+218G>A rs77862416 0.04015
NM_022114.4(PRDM16):c.438+308C>G rs80129380 0.03548
NM_022114.4(PRDM16):c.1187-77T>C rs116395931 0.03123
NM_022114.4(PRDM16):c.*34G>A rs3748837 0.02895
NM_022114.4(PRDM16):c.885-109C>T rs2483220 0.02839
NM_022114.4(PRDM16):c.3696+126G>A rs2493273 0.02738
NM_022114.4(PRDM16):c.1113C>T (p.Cys371=) rs61745281 0.02560
NM_022114.4(PRDM16):c.627C>T (p.His209=) rs12058363 0.02126
NM_022114.4(PRDM16):c.3521+170G>C rs113059246 0.01912
NM_022114.4(PRDM16):c.2793C>T (p.Asn931=) rs59135929 0.01493
NM_022114.4(PRDM16):c.387+167G>T rs114746406 0.01466
NM_022114.4(PRDM16):c.2940-17G>A rs41301967 0.01452
NM_022114.4(PRDM16):c.783C>T (p.Tyr261=) rs61756439 0.00952
NM_022114.4(PRDM16):c.3109+10G>A rs7549401 0.00898
NM_022114.4(PRDM16):c.38-15C>T rs9662053 0.00658
NM_022114.4(PRDM16):c.3369C>T (p.Asp1123=) rs370420046 0.00537
NM_022114.4(PRDM16):c.1212G>A (p.Thr404=) rs139129844 0.00438
NM_022114.4(PRDM16):c.387+6C>T rs369010644 0.00373
NM_022114.4(PRDM16):c.100G>A (p.Ala34Thr) rs187194973 0.00252
NM_022114.4(PRDM16):c.2452G>A (p.Gly818Ser) rs201904226 0.00160
NM_022114.4(PRDM16):c.3102C>T (p.Asn1034=) rs199853370 0.00144
NM_022114.4(PRDM16):c.3687T>C (p.Ala1229=) rs188634763 0.00137
NM_022114.4(PRDM16):c.2379G>A (p.Ser793=) rs368154998 0.00028
NM_022114.4(PRDM16):c.3301G>A (p.Val1101Met) rs201654872 0.00009
GRCh37/hg19 1p36.32(chr1:3057661-3086496)x1
NM_022114.4(PRDM16):c.*73C>T rs2483248
NM_022114.4(PRDM16):c.1032+265G>C rs6424076
NM_022114.4(PRDM16):c.2468G>C (p.Arg823Pro) rs371654192
NM_022114.4(PRDM16):c.2940-36G>T rs41303861
NM_022114.4(PRDM16):c.387+274G>T rs12135062
NM_022114.4(PRDM16):c.573+1410A>G
NM_022114.4(PRDM16):c.884+64_884+94del rs148238606
NM_022114.4(PRDM16):c.884+64_884+94dup rs148238606

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