ClinVar Miner

List of variants in gene combination CFTR, LOC111674472 reported as uncertain significance by Ambry Genetics

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_000492.4(CFTR):c.2991G>C (p.Leu997Phe) rs1800111 0.00208
NM_000492.4(CFTR):c.3041A>G (p.Tyr1014Cys) rs149279509 0.00019
NM_000492.4(CFTR):c.3274T>C (p.Tyr1092His) rs376968326 0.00011
NM_000492.4(CFTR):c.3151A>G (p.Ile1051Val) rs374403559 0.00009
NM_000492.4(CFTR):c.3025G>A (p.Ala1009Thr) rs184724618 0.00008
NM_000492.4(CFTR):c.3289C>T (p.Arg1097Cys) rs201591901 0.00006
NM_000492.4(CFTR):c.3200C>T (p.Ala1067Val) rs1800114 0.00005
NM_000492.4(CFTR):c.3121A>C (p.Lys1041Gln) rs769448889 0.00004
NM_000492.4(CFTR):c.3169A>G (p.Thr1057Ala) rs397508511 0.00004
NM_000492.4(CFTR):c.3322G>C (p.Val1108Leu) rs397508542 0.00004
NM_000492.4(CFTR):c.3038C>A (p.Pro1013His) rs193922516 0.00003
NM_000492.4(CFTR):c.3064G>A (p.Val1022Met) rs144441835 0.00001
NM_000492.4(CFTR):c.3158C>T (p.Thr1053Ile) rs140883683 0.00001
NM_000492.4(CFTR):c.3238A>C (p.Lys1080Gln) rs766126240 0.00001
NM_000492.4(CFTR):c.3267G>C (p.Trp1089Cys) rs150020260 0.00001
NM_000492.4(CFTR):c.3275A>G (p.Tyr1092Cys) rs764434414 0.00001
NM_000492.4(CFTR):c.3350T>C (p.Ile1117Thr) rs751853765 0.00001
NM_000492.4(CFTR):c.2992T>A (p.Leu998Ile) rs2116080345
NM_000492.4(CFTR):c.2994A>C (p.Leu998Phe)
NM_000492.4(CFTR):c.2994A>T (p.Leu998Phe)
NM_000492.4(CFTR):c.3001G>A (p.Val1001Met) rs193922731
NM_000492.4(CFTR):c.3005T>C (p.Ile1002Thr)
NM_000492.4(CFTR):c.3014T>C (p.Ile1005Thr)
NM_000492.4(CFTR):c.3034C>A (p.Gln1012Lys)
NM_000492.4(CFTR):c.3035A>G (p.Gln1012Arg)
NM_000492.4(CFTR):c.3037C>T (p.Pro1013Ser) rs978796108
NM_000492.4(CFTR):c.3038C>T (p.Pro1013Leu) rs193922516
NM_000492.4(CFTR):c.3043A>G (p.Ile1015Val)
NM_000492.4(CFTR):c.3062C>T (p.Pro1021Leu) rs1554392023
NM_000492.4(CFTR):c.3064G>C (p.Val1022Leu) rs144441835
NM_000492.4(CFTR):c.3065T>C (p.Val1022Ala)
NM_000492.4(CFTR):c.3065T>G (p.Val1022Gly)
NM_000492.4(CFTR):c.3070G>A (p.Val1024Met)
NM_000492.4(CFTR):c.3071T>A (p.Val1024Glu)
NM_000492.4(CFTR):c.3073G>T (p.Ala1025Ser)
NM_000492.4(CFTR):c.3076T>G (p.Phe1026Val)
NM_000492.4(CFTR):c.3092C>G (p.Ala1031Gly)
NM_000492.4(CFTR):c.3099C>A (p.Phe1033Leu)
NM_000492.4(CFTR):c.3100C>T (p.Leu1034Phe) rs1554392043
NM_000492.4(CFTR):c.3101T>G (p.Leu1034Arg) rs1792369943
NM_000492.4(CFTR):c.3125A>G (p.Gln1042Arg)
NM_000492.4(CFTR):c.3146G>A (p.Ser1049Asn)
NM_000492.4(CFTR):c.3148C>A (p.Pro1050Thr)
NM_000492.4(CFTR):c.3148C>G (p.Pro1050Ala)
NM_000492.4(CFTR):c.3199G>A (p.Ala1067Thr) rs121909020
NM_000492.4(CFTR):c.3214C>T (p.Pro1072Ser) rs1584822281
NM_000492.4(CFTR):c.3215C>A (p.Pro1072His)
NM_000492.4(CFTR):c.3226A>C (p.Thr1076Pro)
NM_000492.4(CFTR):c.3235C>T (p.His1079Tyr)
NM_000492.4(CFTR):c.3247A>G (p.Asn1083Asp)
NM_000492.4(CFTR):c.3256A>G (p.Thr1086Ala) rs373043500
NM_000492.4(CFTR):c.3256A>T (p.Thr1086Ser) rs373043500
NM_000492.4(CFTR):c.3266G>T (p.Trp1089Leu)
NM_000492.4(CFTR):c.3270C>G (p.Phe1090Leu)
NM_000492.4(CFTR):c.3277C>G (p.Leu1093Val)
NM_000492.4(CFTR):c.3280T>C (p.Ser1094Pro)
NM_000492.4(CFTR):c.3292T>G (p.Trp1098Gly) rs397508531
NM_000492.4(CFTR):c.3299A>C (p.Gln1100Pro) rs397508535
NM_000492.4(CFTR):c.3303G>A (p.Met1101Ile) rs777445862
NM_000492.4(CFTR):c.3306A>C (p.Arg1102Ser)
NM_000492.4(CFTR):c.3308T>G (p.Ile1103Arg)
NM_000492.4(CFTR):c.3322G>A (p.Val1108Ile)
NM_000492.4(CFTR):c.3326T>C (p.Ile1109Thr)
NM_000492.4(CFTR):c.3349A>G (p.Ile1117Val)
NM_000492.4(CFTR):c.3355A>T (p.Ile1119Phe)
NM_000492.4(CFTR):c.3364A>G (p.Thr1122Ala) rs1584822533

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