ClinVar Miner

List of variants in gene CYP4V2 reported as uncertain significance for not provided

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Total variants: 82
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HGVS dbSNP
NC_000004.11:g.(?_187112978)_(187131795_?)dup
NM_207352.4(CYP4V2):c.101T>C (p.Leu34Pro)
NM_207352.4(CYP4V2):c.1049A>G (p.Glu350Gly)
NM_207352.4(CYP4V2):c.1067A>T (p.Asp356Val)
NM_207352.4(CYP4V2):c.1081G>T (p.Asp361Tyr)
NM_207352.4(CYP4V2):c.1120G>T (p.Asp374Tyr)
NM_207352.4(CYP4V2):c.1169G>A (p.Arg390His) rs199476201
NM_207352.4(CYP4V2):c.1198C>T (p.Arg400Cys) rs138444697
NM_207352.4(CYP4V2):c.1229G>T (p.Gly410Val)
NM_207352.4(CYP4V2):c.1249_1250delinsTT (p.Thr417Phe)
NM_207352.4(CYP4V2):c.1273G>A (p.Ala425Thr)
NM_207352.4(CYP4V2):c.1289C>T (p.Pro430Leu) rs144008429
NM_207352.4(CYP4V2):c.1307C>T (p.Pro436Leu)
NM_207352.4(CYP4V2):c.130T>A (p.Trp44Arg) rs119103282
NM_207352.4(CYP4V2):c.1312G>A (p.Glu438Lys)
NM_207352.4(CYP4V2):c.1324G>A (p.Glu442Lys)
NM_207352.4(CYP4V2):c.1327C>T (p.Arg443Trp)
NM_207352.4(CYP4V2):c.1339G>A (p.Glu447Lys) rs200623218
NM_207352.4(CYP4V2):c.1354C>T (p.Arg452Cys)
NM_207352.4(CYP4V2):c.1355G>A (p.Arg452His)
NM_207352.4(CYP4V2):c.1361C>T (p.Pro454Leu)
NM_207352.4(CYP4V2):c.1362A>G (p.Pro454=)
NM_207352.4(CYP4V2):c.1387G>T (p.Gly463Cys)
NM_207352.4(CYP4V2):c.1402A>G (p.Ile468Val)
NM_207352.4(CYP4V2):c.1423A>G (p.Met475Val) rs762821992
NM_207352.4(CYP4V2):c.143G>C (p.Arg48Pro)
NM_207352.4(CYP4V2):c.1441C>G (p.Leu481Val)
NM_207352.4(CYP4V2):c.1444T>C (p.Ser482Pro)
NM_207352.4(CYP4V2):c.1479C>T (p.Asn493=) rs374270799
NM_207352.4(CYP4V2):c.1493A>C (p.Glu498Ala)
NM_207352.4(CYP4V2):c.1495C>T (p.Leu499Phe)
NM_207352.4(CYP4V2):c.14G>C (p.Trp5Ser)
NM_207352.4(CYP4V2):c.1501C>G (p.Leu501Val)
NM_207352.4(CYP4V2):c.1523G>A (p.Arg508His) rs119103284
NM_207352.4(CYP4V2):c.1573C>A (p.Arg525Ser)
NM_207352.4(CYP4V2):c.1573C>T (p.Arg525Cys)
NM_207352.4(CYP4V2):c.169T>C (p.Tyr57His) rs374174110
NM_207352.4(CYP4V2):c.214G>A (p.Glu72Lys)
NM_207352.4(CYP4V2):c.229A>T (p.Ile77Phe)
NM_207352.4(CYP4V2):c.237G>T (p.Glu79Asp) rs199476185
NM_207352.4(CYP4V2):c.263C>T (p.Pro88Leu)
NM_207352.4(CYP4V2):c.263_265del (p.Pro88del)
NM_207352.4(CYP4V2):c.296T>C (p.Met99Thr)
NM_207352.4(CYP4V2):c.302C>T (p.Ala101Val) rs143272248
NM_207352.4(CYP4V2):c.328-3A>G
NM_207352.4(CYP4V2):c.338C>G (p.Thr113Ser)
NM_207352.4(CYP4V2):c.350A>C (p.Gln117Pro)
NM_207352.4(CYP4V2):c.367A>G (p.Met123Val) rs149684063
NM_207352.4(CYP4V2):c.376T>A (p.Phe126Ile)
NM_207352.4(CYP4V2):c.40C>G (p.Leu14Val)
NM_207352.4(CYP4V2):c.422A>G (p.Asn141Ser)
NM_207352.4(CYP4V2):c.430C>T (p.Arg144Cys)
NM_207352.4(CYP4V2):c.431G>A (p.Arg144His)
NM_207352.4(CYP4V2):c.44T>C (p.Leu15Pro)
NM_207352.4(CYP4V2):c.538C>T (p.His180Tyr)
NM_207352.4(CYP4V2):c.541A>G (p.Ile181Val) rs201006021
NM_207352.4(CYP4V2):c.571T>A (p.Tyr191Asn)
NM_207352.4(CYP4V2):c.610G>A (p.Ala204Thr) rs61745524
NM_207352.4(CYP4V2):c.626T>C (p.Ile209Thr) rs376640607
NM_207352.4(CYP4V2):c.674G>C (p.Arg225Thr)
NM_207352.4(CYP4V2):c.684GAT[1] (p.Met229del)
NM_207352.4(CYP4V2):c.686T>C (p.Met229Thr)
NM_207352.4(CYP4V2):c.688A>G (p.Ile230Val)
NM_207352.4(CYP4V2):c.68C>A (p.Ser23Tyr)
NM_207352.4(CYP4V2):c.695G>A (p.Arg232Gln)
NM_207352.4(CYP4V2):c.746AAG[1] (p.Glu250del)
NM_207352.4(CYP4V2):c.772C>A (p.Leu258Ile)
NM_207352.4(CYP4V2):c.780C>G (p.Ile260Met)
NM_207352.4(CYP4V2):c.801+5G>A
NM_207352.4(CYP4V2):c.815G>A (p.Arg272Gln)
NM_207352.4(CYP4V2):c.831C>G (p.Asn277Lys)
NM_207352.4(CYP4V2):c.841G>A (p.Asp281Asn)
NM_207352.4(CYP4V2):c.862G>C (p.Gly288Arg)
NM_207352.4(CYP4V2):c.872C>T (p.Pro291Leu)
NM_207352.4(CYP4V2):c.902A>C (p.Asp301Ala)
NM_207352.4(CYP4V2):c.934A>T (p.Asn312Tyr)
NM_207352.4(CYP4V2):c.951A>C (p.Glu317Asp)
NM_207352.4(CYP4V2):c.962AAG[1] (p.Glu322del)
NM_207352.4(CYP4V2):c.968T>C (p.Val323Ala)
NM_207352.4(CYP4V2):c.974C>T (p.Thr325Ile) rs199476196
NM_207352.4(CYP4V2):c.987+3A>G
NM_207352.4(CYP4V2):c.987+5_987+9del

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