ClinVar Miner

List of variants in gene FLVCR1 reported as benign for cerebellar degeneration

Included ClinVar conditions (265):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_014053.4(FLVCR1):c.*1151A>G rs6682947 0.60512
NM_014053.4(FLVCR1):c.*339T>G rs12074192 0.60505
NM_014053.4(FLVCR1):c.*1609A>G rs12405742 0.59824
NM_014053.4(FLVCR1):c.-86C>T rs2201603 0.45780
NM_014053.4(FLVCR1):c.*2813G>A rs1284854 0.45117
NM_014053.4(FLVCR1):c.*2578G>A rs1284856 0.42748
NM_014053.4(FLVCR1):c.*2709T>C rs1284855 0.42731
NM_014053.4(FLVCR1):c.1631C>T (p.Thr544Met) rs3207090 0.38895
NM_014053.4(FLVCR1):c.*1826C>T rs12567976 0.38865
NM_014053.4(FLVCR1):c.*2419G>A rs10864027 0.38756
NM_014053.4(FLVCR1):c.*1793C>T rs12567975 0.38742
NM_014053.4(FLVCR1):c.*788C>T rs6670064 0.36556
NM_014053.4(FLVCR1):c.*626T>A rs11582817 0.36511
NM_014053.4(FLVCR1):c.*844T>C rs12565125 0.22460
NM_014053.4(FLVCR1):c.*931C>T rs12567713 0.21766
NM_014053.4(FLVCR1):c.1307+19T>A rs2291772 0.21660
NM_014053.4(FLVCR1):c.*1106C>T rs12567728 0.21651
NM_014053.4(FLVCR1):c.*673G>A rs41301027 0.21642
NM_014053.4(FLVCR1):c.1593+9T>C rs17019870 0.21623
NM_014053.4(FLVCR1):c.*2968G>A rs10902 0.21622
NM_014053.4(FLVCR1):c.*2908G>A rs1284853 0.21097
NM_014053.4(FLVCR1):c.*3313G>T rs15903 0.21069
NM_014053.4(FLVCR1):c.*1600G>A rs55793082 0.16870
NM_014053.4(FLVCR1):c.*1940G>A rs6697126 0.09080
NM_014053.4(FLVCR1):c.*353A>G rs6679775 0.08452
NM_014053.4(FLVCR1):c.*1751C>T rs187971996 0.02794
NM_014053.4(FLVCR1):c.1272T>C (p.Tyr424=) rs17677416 0.02755
NM_014053.4(FLVCR1):c.*377T>C rs41258034 0.02608
NM_014053.4(FLVCR1):c.*891A>G rs41301029 0.02342
NM_014053.4(FLVCR1):c.*855T>C rs564661630 0.01999
NM_014053.4(FLVCR1):c.*1544A>G rs6685793 0.00936
NM_014053.4(FLVCR1):c.*500G>A rs41301023 0.00597
NM_014053.4(FLVCR1):c.*3241C>T rs113198161 0.00493
NM_014053.4(FLVCR1):c.*1317A>G rs145011972 0.00394
NM_014053.4(FLVCR1):c.*3032G>T rs76321605 0.00330
NM_014053.4(FLVCR1):c.*2540T>C rs79275553 0.00322
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550 0.00251
NM_014053.4(FLVCR1):c.*279T>C rs17019875 0.00084
NM_014053.4(FLVCR1):c.*2443C>T rs117380165 0.00056
NM_014053.4(FLVCR1):c.*1920T>A rs115914498 0.00052
NM_014053.4(FLVCR1):c.*3264T>C rs374214375 0.00005
NM_014053.4(FLVCR1):c.*1880TAAA[7] rs141272551
NM_014053.4(FLVCR1):c.*2061CA[12] rs139242973
NM_014053.4(FLVCR1):c.*3130_*3131insAATT rs10655434
NM_014053.4(FLVCR1):c.*3482C>G rs12142813
NM_014053.4(FLVCR1):c.1413+82TTG[6] rs41300975
NM_014053.4(FLVCR1):c.1594-13_1594-10dup rs41301015

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