ClinVar Miner

List of variants reported as not provided by Molecular Psychiatry Laboratory, RIKEN

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Total variants: 35
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HGVS dbSNP
NM_001444.3(FABP5):c.279A>G (p.Ala93=) rs431905489
NM_001444.3(FABP5):c.331T>C (p.Leu111=) rs431905490
NM_001444.3(FABP5):c.371A>G (p.Asn124Ser) rs431905491
NM_001446.5(FABP7):c.239del (p.Asn80fs) rs431905492
NM_004102.5(FABP3):c.246+16_246+17del rs483352874
NM_004102.5(FABP3):c.246+25del rs431905487
NM_004102.5(FABP3):c.349-14_349-13del rs483352875
NM_004102.5(FABP3):c.349-19A>G rs431905488
NM_004102.5(FABP3):c.395del (p.Glu132fs) rs483352865
NM_005094.4(SLC27A4):c.*23C>T rs587777865
NM_005094.4(SLC27A4):c.1237G>A (p.Val413Met) rs367871179
NM_005094.4(SLC27A4):c.13G>T (p.Ala5Ser) rs587776375
NM_005094.4(SLC27A4):c.1440G>A (p.Lys480=) rs587776382
NM_005094.4(SLC27A4):c.1462+25C>T rs587776383
NM_005094.4(SLC27A4):c.1504C>T (p.Arg502Ter) rs587776384
NM_005094.4(SLC27A4):c.1575C>T (p.Leu525=) rs587776373
NM_005094.4(SLC27A4):c.1775-13C>T rs587776374
NM_005094.4(SLC27A4):c.1881G>A (p.Pro627=) rs587776385
NM_005094.4(SLC27A4):c.1904G>A (p.Arg635His) rs587776386
NM_005094.4(SLC27A4):c.250G>A (p.Val84Ile) rs587776372
NM_005094.4(SLC27A4):c.352C>T (p.Leu118=) rs587776376
NM_005094.4(SLC27A4):c.513C>G (p.Thr171=) rs587776377
NM_005094.4(SLC27A4):c.519C>T (p.Arg173=) rs587776378
NM_005094.4(SLC27A4):c.523C>T (p.Arg175Trp) rs587776379
NM_005094.4(SLC27A4):c.716-16C>T rs587777746
NM_005094.4(SLC27A4):c.823C>T (p.Arg275Cys) rs587776380
NM_024330.4(SLC27A3):c.1161+5G>A rs149362751
NM_024330.4(SLC27A3):c.1447+19G>A rs146145258
NM_024330.4(SLC27A3):c.1447+1G>A rs142223071
NM_024330.4(SLC27A3):c.1875+15C>A rs146389904
NM_024330.4(SLC27A3):c.1876-11C>G rs148593808
NM_024330.4(SLC27A3):c.188G>T (p.Gly63Val) rs34527123
NM_024330.4(SLC27A3):c.667+24C>T rs140194614
NM_024330.4(SLC27A3):c.668-24C>T rs143973304
NM_024330.4(SLC27A3):c.878-24C>T rs151180786

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