ClinVar Miner

List of variants in gene FRMPD4 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_001368397.1(FRMPD4):c.3899C>A (p.Thr1300Asn) rs139367112 0.00175
NM_001368397.1(FRMPD4):c.3703G>A (p.Val1235Met) rs143569009 0.00053
NM_001368397.1(FRMPD4):c.3260G>A (p.Arg1087His) rs769071295 0.00023
NM_001368397.1(FRMPD4):c.1736C>T (p.Thr579Met) rs149409320 0.00020
NM_001368397.1(FRMPD4):c.1021G>A (p.Ala341Thr) rs142194011 0.00016
NM_001368397.1(FRMPD4):c.1925C>T (p.Ala642Val) rs142025193 0.00011
NM_001368397.1(FRMPD4):c.2200C>T (p.Pro734Ser) rs201325065 0.00010
NM_001368397.1(FRMPD4):c.1636C>T (p.Leu546Phe) rs200271818 0.00007
NM_001368397.1(FRMPD4):c.2903C>T (p.Ser968Leu) rs146907470 0.00006
NM_001368397.1(FRMPD4):c.3067T>C (p.Cys1023Arg) rs143929343 0.00005
NM_001368397.1(FRMPD4):c.2048A>G (p.Glu683Gly) rs760597864 0.00004
NM_001368397.1(FRMPD4):c.2605G>A (p.Val869Ile) rs146534723 0.00004
NM_001368397.1(FRMPD4):c.3938G>A (p.Arg1313Gln) rs759503727 0.00004
NM_001368397.1(FRMPD4):c.2003C>A (p.Thr668Asn) rs376545795 0.00003
NM_001368397.1(FRMPD4):c.2569G>A (p.Ala857Thr) rs368784263 0.00003
NM_001368397.1(FRMPD4):c.3766G>A (p.Val1256Met) rs1036437887 0.00003
NM_001368397.1(FRMPD4):c.1757C>T (p.Thr586Ile) rs779000840 0.00002
NM_001368397.1(FRMPD4):c.1790T>C (p.Ile597Thr) rs757866192 0.00002
NM_001368397.1(FRMPD4):c.125C>T (p.Thr42Met) rs146122430 0.00001
NM_001368397.1(FRMPD4):c.2784G>T (p.Gln928His) rs777248043 0.00001
NM_001368397.1(FRMPD4):c.3097G>A (p.Asp1033Asn) rs772365939 0.00001
NM_001368397.1(FRMPD4):c.2081A>G (p.Asn694Ser)
NM_001368397.1(FRMPD4):c.2182G>A (p.Ala728Thr) rs750615873
NM_001368397.1(FRMPD4):c.221C>T (p.Pro74Leu)
NM_001368397.1(FRMPD4):c.2243C>G (p.Ala748Gly) rs370344979
NM_001368397.1(FRMPD4):c.2428C>G (p.Pro810Ala)
NM_001368397.1(FRMPD4):c.3161C>T (p.Thr1054Met)
NM_001368397.1(FRMPD4):c.3268A>G (p.Ser1090Gly)
NM_001368397.1(FRMPD4):c.3428G>T (p.Gly1143Val)
NM_001368397.1(FRMPD4):c.3682G>A (p.Gly1228Ser) rs140005767
NM_001368397.1(FRMPD4):c.3814G>A (p.Gly1272Arg)
NM_001368397.1(FRMPD4):c.50C>T (p.Thr17Met)
NM_001368397.1(FRMPD4):c.77C>T (p.Ser26Leu)

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