ClinVar Miner

List of variants in gene CCDC141 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_173648.4(CCDC141):c.4369G>A (p.Val1457Ile) rs145610810 0.00504
NM_173648.4(CCDC141):c.1521A>C (p.Gln507His) rs114129666 0.00468
NM_173648.4(CCDC141):c.2299G>A (p.Asp767Asn) rs141939661 0.00367
NM_173648.4(CCDC141):c.2614C>G (p.Leu872Val) rs144766496 0.00225
NM_173648.4(CCDC141):c.3111A>T (p.Lys1037Asn) rs149198764 0.00177
NM_173648.4(CCDC141):c.1707G>A (p.Lys569=) rs192561722 0.00170
NM_173648.4(CCDC141):c.1461T>C (p.Val487=) rs201327469 0.00125
NM_173648.4(CCDC141):c.202G>A (p.Glu68Lys) rs540836199 0.00125
NM_173648.4(CCDC141):c.4160T>C (p.Val1387Ala) rs148579179 0.00101
NM_173648.4(CCDC141):c.1719+7T>C rs13019863 0.00081
NM_173648.4(CCDC141):c.3500T>A (p.Leu1167Ter) rs139096421 0.00054
NM_173648.4(CCDC141):c.1755T>C (p.Tyr585=) rs141916607 0.00028
NM_173648.4(CCDC141):c.1587A>G (p.Val529=) rs370398580 0.00024
NM_173648.4(CCDC141):c.3303T>C (p.Leu1101=) rs369890692 0.00020
NM_173648.4(CCDC141):c.3060+19G>T rs368755845 0.00017
NM_173648.4(CCDC141):c.867T>C (p.His289=) rs372474638 0.00009
NM_173648.4(CCDC141):c.1225C>T (p.Gln409Ter) rs143025382 0.00007
NM_173648.4(CCDC141):c.1059G>C (p.Lys353Asn) rs1391287036 0.00006
NM_173648.4(CCDC141):c.2310C>T (p.His770=) rs200376493 0.00006
NM_173648.4(CCDC141):c.1093-7T>G rs199660822 0.00004
NM_173648.4(CCDC141):c.1278C>T (p.Ser426=) rs749928552 0.00004
NM_173648.4(CCDC141):c.2346C>T (p.Tyr782=) rs150796414 0.00004
NM_173648.4(CCDC141):c.2799A>G (p.Lys933=) rs529109294 0.00004
NM_173648.4(CCDC141):c.3630A>G (p.Ser1210=) rs150972468 0.00004
NM_173648.4(CCDC141):c.1621A>C (p.Arg541=) rs575883722 0.00002
NM_173648.4(CCDC141):c.3627C>T (p.Val1209=) rs990151073 0.00002
NM_173648.4(CCDC141):c.1512A>C (p.Leu504=) rs186331250 0.00001
NM_173648.4(CCDC141):c.1683G>A (p.Leu561=) rs927852845 0.00001
NM_173648.4(CCDC141):c.229T>C (p.Leu77=) rs1016557316 0.00001
NM_173648.4(CCDC141):c.2496A>G (p.Glu832=) rs1369334354 0.00001
NM_173648.4(CCDC141):c.2592T>C (p.Ser864=) rs768088717 0.00001
NM_173648.4(CCDC141):c.3075C>T (p.Tyr1025=) rs370006865 0.00001
NM_173648.4(CCDC141):c.3753G>A (p.Val1251=) rs185286713 0.00001
NM_173648.4(CCDC141):c.553T>C (p.Leu185=) rs781075626 0.00001
NM_173648.4(CCDC141):c.102+16C>T
NM_173648.4(CCDC141):c.1600G>A (p.Val534Ile)
NM_173648.4(CCDC141):c.1815G>A (p.Ser605=)
NM_173648.4(CCDC141):c.2268C>T (p.Ala756=)
NM_173648.4(CCDC141):c.252C>T (p.Leu84=)
NM_173648.4(CCDC141):c.2595A>G (p.Ala865=)
NM_173648.4(CCDC141):c.2606A>G (p.Gln869Arg)
NM_173648.4(CCDC141):c.2637C>T (p.Ser879=)
NM_173648.4(CCDC141):c.2673G>T (p.Arg891=)
NM_173648.4(CCDC141):c.2676C>T (p.Thr892=)
NM_173648.4(CCDC141):c.2679G>T (p.Leu893=)
NM_173648.4(CCDC141):c.2701G>A (p.Ala901Thr)
NM_173648.4(CCDC141):c.2745T>C (p.Asp915=)
NM_173648.4(CCDC141):c.2766T>C (p.Asn922=)
NM_173648.4(CCDC141):c.2865+13T>C
NM_173648.4(CCDC141):c.2934T>C (p.Asp978=)
NM_173648.4(CCDC141):c.3076G>A (p.Glu1026Lys)
NM_173648.4(CCDC141):c.3126C>T (p.Cys1042=)
NM_173648.4(CCDC141):c.3191C>T (p.Pro1064Leu)
NM_173648.4(CCDC141):c.3192G>A (p.Pro1064=)
NM_173648.4(CCDC141):c.3198A>G (p.Gln1066=)
NM_173648.4(CCDC141):c.3245-9C>G rs1170263217
NM_173648.4(CCDC141):c.3342C>A (p.Leu1114=)
NM_173648.4(CCDC141):c.3474+17A>C
NM_173648.4(CCDC141):c.3687A>G (p.Pro1229=)
NM_173648.4(CCDC141):c.3879G>A (p.Gln1293=)
NM_173648.4(CCDC141):c.3915C>T (p.Phe1305=)
NM_173648.4(CCDC141):c.4107C>T (p.Phe1369=)
NM_173648.4(CCDC141):c.420T>C (p.Phe140=)
NM_173648.4(CCDC141):c.4260C>A (p.Val1420=) rs1575112506
NM_173648.4(CCDC141):c.4383G>A (p.Glu1461=)
NM_173648.4(CCDC141):c.4539C>T (p.Thr1513=) rs1324936014
NM_173648.4(CCDC141):c.576T>C (p.Thr192=)
NM_173648.4(CCDC141):c.599G>T (p.Cys200Phe)
NM_173648.4(CCDC141):c.681A>G (p.Leu227=)
NM_173648.4(CCDC141):c.780+16A>G
NM_173648.4(CCDC141):c.897+8A>T

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