ClinVar Miner

List of variants in gene PRDM16 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_022114.4(PRDM16):c.1212G>A (p.Thr404=) rs139129844 0.00438
NM_022114.4(PRDM16):c.2506G>A (p.Gly836Ser) rs114204766 0.00168
NM_022114.4(PRDM16):c.1426C>T (p.Pro476Ser) rs188908415 0.00131
NM_022114.4(PRDM16):c.1134C>G (p.Ser378=) rs200169663 0.00088
NM_022114.4(PRDM16):c.2634C>T (p.Pro878=) rs201338158 0.00065
NM_022114.4(PRDM16):c.2406G>A (p.Pro802=) rs368750536 0.00063
NM_022114.4(PRDM16):c.2603+6C>T rs374549827 0.00058
NM_022114.4(PRDM16):c.2142G>A (p.Lys714=) rs200167919 0.00041
NM_022114.4(PRDM16):c.2508C>T (p.Gly836=) rs374271999 0.00035
NM_022114.4(PRDM16):c.2187C>G (p.Phe729Leu) rs200109766 0.00033
NM_022114.4(PRDM16):c.2281G>A (p.Ala761Thr) rs200947814 0.00029
NM_022114.4(PRDM16):c.252C>T (p.Phe84=) rs370290776 0.00017
NM_022114.4(PRDM16):c.1574G>A (p.Arg525Gln) rs373011563 0.00013
NM_022114.4(PRDM16):c.2223G>A (p.Thr741=) rs756779855 0.00010
NM_022114.4(PRDM16):c.2503G>A (p.Ala835Thr) rs755872965 0.00009
NM_022114.4(PRDM16):c.1614C>A (p.Pro538=) rs375659212 0.00008
NM_022114.4(PRDM16):c.2814G>A (p.Thr938=) rs140540302 0.00007
NM_022114.4(PRDM16):c.3135G>A (p.Thr1045=) rs761078027 0.00007
NM_022114.4(PRDM16):c.2295C>T (p.Gly765=) rs376224745 0.00006
NM_022114.4(PRDM16):c.3405C>T (p.Ala1135=) rs765114438 0.00005
NM_022114.4(PRDM16):c.1170G>A (p.Thr390=) rs374263452 0.00002
NM_022114.4(PRDM16):c.3210C>T (p.Asp1070=) rs1408885025 0.00001
NM_022114.4(PRDM16):c.2448C>T (p.Asn816=) rs372189819
NM_022114.4(PRDM16):c.3237T>C (p.Phe1079=)

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