ClinVar Miner

List of variants in gene FLAD1 reported as likely benign for not provided

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Gene type:
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Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_025207.5(FLAD1):c.373-516G>A rs113906979 0.01295
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 0.00496
NM_025207.5(FLAD1):c.1310G>A (p.Arg437His) rs144820916 0.00210
NM_025207.5(FLAD1):c.729C>T (p.Phe243=) rs61736264 0.00195
NM_025207.5(FLAD1):c.1118-33C>T rs191570212 0.00177
NM_025207.5(FLAD1):c.683G>A (p.Arg228His) rs144986636 0.00093
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.443G>A (p.Arg148Gln) rs140409443 0.00040
NM_025207.5(FLAD1):c.645A>G (p.Glu215=) rs138843652 0.00040
NM_025207.5(FLAD1):c.1566C>T (p.Tyr522=) rs148439225 0.00023
NM_025207.5(FLAD1):c.1495T>C (p.Cys499Arg) rs141604312 0.00014
NM_025207.5(FLAD1):c.1071C>T (p.Asn357=) rs371405282 0.00009
NM_025207.5(FLAD1):c.1614C>T (p.Ile538=) rs139255409 0.00006
NM_025207.5(FLAD1):c.1265+15G>A rs754741967 0.00004
NM_025207.5(FLAD1):c.1555-19T>G rs369848433 0.00004
NM_025207.5(FLAD1):c.1738G>A (p.Glu580Lys) rs186635615 0.00004
NM_025207.5(FLAD1):c.1530A>G (p.Ala510=) rs570971151 0.00003
NM_025207.5(FLAD1):c.627C>T (p.Thr209=) rs748480567 0.00003
NM_025207.5(FLAD1):c.1023C>T (p.Tyr341=) rs1054241904 0.00002
NM_025207.5(FLAD1):c.1150C>T (p.Leu384=) rs535077896 0.00002
NM_025207.5(FLAD1):c.372+10G>A rs752881063 0.00002
NM_025207.5(FLAD1):c.1212C>T (p.Asn404=) rs751432092 0.00001
NM_025207.5(FLAD1):c.1365-9C>T rs769041421 0.00001
NM_025207.5(FLAD1):c.1599T>C (p.Phe533=) rs761280560 0.00001
NM_025207.5(FLAD1):c.373-14C>G rs780088175 0.00001
NM_025207.5(FLAD1):c.609C>T (p.Pro203=) rs776874328 0.00001
NM_025207.5(FLAD1):c.1002C>A (p.Pro334=) rs770776511
NM_025207.5(FLAD1):c.1014C>T (p.Cys338=)
NM_025207.5(FLAD1):c.1107C>T (p.Leu369=)
NM_025207.5(FLAD1):c.1110T>C (p.Ala370=)
NM_025207.5(FLAD1):c.1117+10T>A
NM_025207.5(FLAD1):c.1117+16A>G
NM_025207.5(FLAD1):c.1117+20G>C
NM_025207.5(FLAD1):c.1118-17C>A
NM_025207.5(FLAD1):c.1118-7T>A
NM_025207.5(FLAD1):c.1118-8C>G
NM_025207.5(FLAD1):c.1126T>C (p.Leu376=)
NM_025207.5(FLAD1):c.1131G>A (p.Gly377=)
NM_025207.5(FLAD1):c.1173G>A (p.Leu391=)
NM_025207.5(FLAD1):c.120C>G (p.Leu40=) rs2102235746
NM_025207.5(FLAD1):c.1237C>T (p.Leu413=)
NM_025207.5(FLAD1):c.1242C>T (p.His414=)
NM_025207.5(FLAD1):c.1265+10C>T
NM_025207.5(FLAD1):c.1265+14C>G
NM_025207.5(FLAD1):c.1265+14C>T
NM_025207.5(FLAD1):c.1329T>C (p.Pro443=)
NM_025207.5(FLAD1):c.1359C>A (p.Ile453=)
NM_025207.5(FLAD1):c.1364+12C>A
NM_025207.5(FLAD1):c.1364+12C>G
NM_025207.5(FLAD1):c.1364+21del
NM_025207.5(FLAD1):c.1365-13G>A
NM_025207.5(FLAD1):c.1381T>C (p.Leu461=)
NM_025207.5(FLAD1):c.1443G>A (p.Leu481=)
NM_025207.5(FLAD1):c.1485C>G (p.Ser495=)
NM_025207.5(FLAD1):c.1488T>C (p.Cys496=)
NM_025207.5(FLAD1):c.1509C>T (p.Pro503=)
NM_025207.5(FLAD1):c.1518A>G (p.Pro506=)
NM_025207.5(FLAD1):c.1527C>G (p.Pro509=)
NM_025207.5(FLAD1):c.1527C>T (p.Pro509=)
NM_025207.5(FLAD1):c.1551G>A (p.Leu517=)
NM_025207.5(FLAD1):c.1554+12G>T
NM_025207.5(FLAD1):c.1555-156A>G
NM_025207.5(FLAD1):c.1555-4C>T
NM_025207.5(FLAD1):c.1581T>C (p.Asp527=)
NM_025207.5(FLAD1):c.1587G>A (p.Leu529=)
NM_025207.5(FLAD1):c.1628+13G>C
NM_025207.5(FLAD1):c.1628+18A>G
NM_025207.5(FLAD1):c.1629-10C>G
NM_025207.5(FLAD1):c.1629-13C>T
NM_025207.5(FLAD1):c.1632C>T (p.Tyr544=)
NM_025207.5(FLAD1):c.1671G>A (p.Pro557=)
NM_025207.5(FLAD1):c.1677G>A (p.Leu559=)
NM_025207.5(FLAD1):c.168C>T (p.Pro56=)
NM_025207.5(FLAD1):c.1731G>A (p.Glu577=)
NM_025207.5(FLAD1):c.1734C>T (p.Asn578=)
NM_025207.5(FLAD1):c.1758C>T (p.Arg586=)
NM_025207.5(FLAD1):c.1761A>G (p.Thr587=)
NM_025207.5(FLAD1):c.186C>G (p.Gly62=)
NM_025207.5(FLAD1):c.189C>G (p.Pro63=)
NM_025207.5(FLAD1):c.192G>A (p.Gln64=)
NM_025207.5(FLAD1):c.198T>C (p.Pro66=)
NM_025207.5(FLAD1):c.207G>A (p.Leu69=)
NM_025207.5(FLAD1):c.207G>C (p.Leu69=)
NM_025207.5(FLAD1):c.216C>T (p.Pro72=)
NM_025207.5(FLAD1):c.232C>T (p.Leu78=)
NM_025207.5(FLAD1):c.264C>T (p.Ala88=)
NM_025207.5(FLAD1):c.282A>G (p.Glu94=)
NM_025207.5(FLAD1):c.300T>G (p.Ser100=)
NM_025207.5(FLAD1):c.339T>C (p.Ala113=)
NM_025207.5(FLAD1):c.360T>C (p.Asp120=)
NM_025207.5(FLAD1):c.36G>A (p.Arg12=)
NM_025207.5(FLAD1):c.372+12A>C
NM_025207.5(FLAD1):c.372+14A>C
NM_025207.5(FLAD1):c.372+24_372+25del rs34858109
NM_025207.5(FLAD1):c.373-14C>T
NM_025207.5(FLAD1):c.373-5C>T
NM_025207.5(FLAD1):c.373-7C>T rs2102244210
NM_025207.5(FLAD1):c.387C>T (p.Asp129=)
NM_025207.5(FLAD1):c.414A>G (p.Thr138=)
NM_025207.5(FLAD1):c.435G>A (p.Gln145=)
NM_025207.5(FLAD1):c.441C>T (p.Cys147=)
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.525A>G (p.Thr175=)
NM_025207.5(FLAD1):c.537C>T (p.Ile179=)
NM_025207.5(FLAD1):c.558G>A (p.Val186=)
NM_025207.5(FLAD1):c.573G>C (p.Val191=) rs1657709721
NM_025207.5(FLAD1):c.648C>A (p.Gly216=)
NM_025207.5(FLAD1):c.664T>C (p.Leu222=)
NM_025207.5(FLAD1):c.696C>T (p.Gly232=)
NM_025207.5(FLAD1):c.711T>C (p.Thr237=)
NM_025207.5(FLAD1):c.717A>G (p.Gln239=)
NM_025207.5(FLAD1):c.735G>A (p.Leu245=)
NM_025207.5(FLAD1):c.750C>T (p.Asn250=)
NM_025207.5(FLAD1):c.78G>A (p.Lys26=)
NM_025207.5(FLAD1):c.798G>A (p.Glu266=) rs533763383
NM_025207.5(FLAD1):c.849G>A (p.Glu283=)
NM_025207.5(FLAD1):c.921G>A (p.Arg307=)
NM_025207.5(FLAD1):c.951C>A (p.Gly317=)
NM_025207.5(FLAD1):c.972G>A (p.Lys324=)

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