ClinVar Miner

List of variants in gene FLAD1 reported by GeneDx

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_025207.4(FLAD1):c.-447C>T rs10908449 0.15318
NM_025207.5(FLAD1):c.1555-259_1555-256dup rs10683289 0.14814
NM_025207.5(FLAD1):c.373-699A>G rs7525580 0.13333
NM_025207.5(FLAD1):c.373-562T>G rs7528060 0.12972
NM_025207.5(FLAD1):c.1118-330A>G rs2089248 0.09882
NM_025207.5(FLAD1):c.372+120C>A rs6696397 0.05871
NM_025207.5(FLAD1):c.1117+123T>G rs2089247 0.04547
NM_025207.5(FLAD1):c.1117+133A>G rs2878517 0.04546
NM_025207.5(FLAD1):c.372+218G>C rs78191343 0.04203
NM_025207.5(FLAD1):c.1555-76G>T rs7535144 0.03711
NM_025207.5(FLAD1):c.373-516G>A rs113906979 0.01194
NM_025207.5(FLAD1):c.372+186C>G rs78605724 0.01098
NM_025207.5(FLAD1):c.1555-235C>A rs114503518 0.01095
NM_025207.5(FLAD1):c.1118-163_1118-162del rs372031707 0.00448
NM_025207.5(FLAD1):c.1310G>A (p.Arg437His) rs144820916 0.00210
NM_025207.5(FLAD1):c.1118-33C>T rs191570212 0.00177
NM_025207.5(FLAD1):c.729C>T (p.Phe243=) rs61736264 0.00173
NM_025207.5(FLAD1):c.-27A>G rs373075625 0.00091
NM_025207.5(FLAD1):c.683G>A (p.Arg228His) rs144986636 0.00088
NM_025207.5(FLAD1):c.1119G>A (p.Gly373=) rs142224458 0.00083
NM_025207.5(FLAD1):c.1309C>T (p.Arg437Cys) rs146865554 0.00077
NM_025207.5(FLAD1):c.787C>T (p.Arg263Trp) rs146501091 0.00075
NM_025207.5(FLAD1):c.640G>A (p.Gly214Arg) rs145054820 0.00074
NM_025207.5(FLAD1):c.1184G>A (p.Ser395Asn) rs146796757 0.00049
NM_025207.5(FLAD1):c.1033C>T (p.Arg345Cys) rs61740252 0.00042
NM_025207.5(FLAD1):c.645A>G (p.Glu215=) rs138843652 0.00039
NM_025207.5(FLAD1):c.1589G>A (p.Arg530His) rs146007674 0.00025
NM_025207.5(FLAD1):c.203A>G (p.Asp68Gly) rs150060495 0.00024
NM_025207.5(FLAD1):c.1566C>T (p.Tyr522=) rs148439225 0.00023
NM_025207.5(FLAD1):c.210dup (p.Gly71fs) rs544864359 0.00022
NM_025207.5(FLAD1):c.410G>A (p.Arg137Gln) rs61741145 0.00010
NM_025207.5(FLAD1):c.1469G>A (p.Arg490Gln) rs201707334 0.00009
NM_025207.5(FLAD1):c.97G>A (p.Gly33Arg) rs142890812 0.00009
NM_025207.5(FLAD1):c.130C>T (p.Leu44Phe) rs146082473 0.00008
NM_025207.5(FLAD1):c.917G>A (p.Arg306His) rs200154742 0.00006
NM_025207.5(FLAD1):c.1049C>T (p.Ser350Leu) rs757699721 0.00005
NM_025207.5(FLAD1):c.1588C>T (p.Arg530Cys) rs771466122 0.00005
NM_025207.5(FLAD1):c.580G>T (p.Ala194Ser) rs1250036112 0.00005
NM_025207.5(FLAD1):c.1157C>T (p.Thr386Ile) rs769162563 0.00004
NM_025207.5(FLAD1):c.1555-19T>G rs369848433 0.00004
NM_025207.5(FLAD1):c.788G>A (p.Arg263Gln) rs566351390 0.00004
NM_025207.5(FLAD1):c.1555-10G>A rs1227440416 0.00003
NM_025207.5(FLAD1):c.408C>A (p.Cys136Ter) rs1057518160 0.00002
NM_025207.5(FLAD1):c.-304C>T rs537748007 0.00001
NM_025207.5(FLAD1):c.1167C>T (p.Thr389=) rs368097196 0.00001
NM_025207.5(FLAD1):c.1212C>T (p.Asn404=) rs751432092 0.00001
NM_025207.5(FLAD1):c.1664G>A (p.Arg555Gln) rs2232633 0.00001
NM_025207.5(FLAD1):c.445G>A (p.Val149Ile) rs755926549 0.00001
NC_000001.11:g.154982978_154982979insGGGC rs150880165
NM_025207.5(FLAD1):c.-294AG[1] rs569007120
NM_025207.5(FLAD1):c.1054_1075del (p.Val352fs) rs1170313629
NM_025207.5(FLAD1):c.1229C>A (p.Thr410Asn)
NM_025207.5(FLAD1):c.1389_1398del (p.Ala463_Glu464insTer) rs1571488364
NM_025207.5(FLAD1):c.1619A>G (p.Tyr540Cys)
NM_025207.5(FLAD1):c.245T>C (p.Leu82Pro)
NM_025207.5(FLAD1):c.270G>C (p.Gln90His)
NM_025207.5(FLAD1):c.292A>G (p.Met98Val) rs1657447676
NM_025207.5(FLAD1):c.35G>A (p.Arg12Lys)
NM_025207.5(FLAD1):c.503A>G (p.Asn168Ser) rs150372864
NM_025207.5(FLAD1):c.503A>T (p.Asn168Ile) rs150372864
NM_025207.5(FLAD1):c.708C>A (p.Cys236Ter) rs1657717722
NM_025207.5(FLAD1):c.844A>G (p.Lys282Glu)
NM_025207.5(FLAD1):c.853T>C (p.Tyr285His)

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