ClinVar Miner

List of variants in gene RAB7A reported as uncertain significance for Charcot-Marie-Tooth disease type 2

Included ClinVar conditions (92):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_004637.6(RAB7A):c.*181G>A rs3206306 0.03706
NM_004637.6(RAB7A):c.*183A>G rs774054837 0.03357
NM_004637.6(RAB7A):c.*85A>G rs549333234 0.00085
NM_004637.6(RAB7A):c.*274G>A rs565849348 0.00083
NM_004637.6(RAB7A):c.*402T>A rs950767971 0.00021
NM_004637.6(RAB7A):c.*1142G>A rs747470481 0.00009
NM_004637.6(RAB7A):c.*989C>G rs1039323764 0.00009
NM_004637.6(RAB7A):c.*165A>T rs886057942 0.00007
NM_004637.6(RAB7A):c.*1029A>G rs776759455 0.00006
NM_004637.6(RAB7A):c.*1301A>G rs182528613 0.00004
NM_004637.6(RAB7A):c.*956G>A rs1421148594 0.00004
NM_004637.6(RAB7A):c.-18A>G rs886057941 0.00004
NM_004637.6(RAB7A):c.*1344G>A rs763557372 0.00003
NM_004637.6(RAB7A):c.506T>C (p.Ile169Thr) rs375630134 0.00003
NM_004637.6(RAB7A):c.*1343C>T rs576597041 0.00002
NM_004637.6(RAB7A):c.*702T>G rs886057947 0.00002
NM_004637.6(RAB7A):c.167T>C (p.Leu56Pro) rs775104487 0.00002
NM_004637.6(RAB7A):c.508G>A (p.Ala170Thr) rs750766845 0.00002
NM_004637.6(RAB7A):c.*831A>G rs1432428820 0.00001
NM_004637.6(RAB7A):c.152T>C (p.Met51Thr) rs769771992 0.00001
NM_004637.6(RAB7A):c.481A>G (p.Asn161Asp) rs963894786 0.00001
NM_004637.6(RAB7A):c.482A>G (p.Asn161Ser) rs121909080 0.00001
NM_004637.5(RAB7A):c.-204G>T rs886057938
NM_004637.5(RAB7A):c.-209_-204dup rs770559386
NM_004637.6(RAB7A):c.*1079C>T rs141066124
NM_004637.6(RAB7A):c.*1161C>T rs886057952
NM_004637.6(RAB7A):c.*1219C>T rs1036501286
NM_004637.6(RAB7A):c.*182CA[9] rs139417205
NM_004637.6(RAB7A):c.*317A>G rs1933980298
NM_004637.6(RAB7A):c.*421_*423del rs886057944
NM_004637.6(RAB7A):c.*473G>C rs886057945
NM_004637.6(RAB7A):c.*700C>T rs886057946
NM_004637.6(RAB7A):c.*801dup rs886057948
NM_004637.6(RAB7A):c.*819C>A rs772662283
NM_004637.6(RAB7A):c.*908A>C rs546868558
NM_004637.6(RAB7A):c.*922A>G rs886057949
NM_004637.6(RAB7A):c.*929A>T rs886057950
NM_004637.6(RAB7A):c.*974A>G rs1933994920
NM_004637.6(RAB7A):c.*997T>G rs3755593
NM_004637.6(RAB7A):c.-146G>C rs1044292082
NM_004637.6(RAB7A):c.-154G>A rs886057939
NM_004637.6(RAB7A):c.-61G>A rs2070377358
NM_004637.6(RAB7A):c.-70CTC[2] rs763539443
NM_004637.6(RAB7A):c.148G>A (p.Val50Met) rs1933610846
NM_004637.6(RAB7A):c.151A>G (p.Met51Val)
NM_004637.6(RAB7A):c.180+4A>T rs1933611370
NM_004637.6(RAB7A):c.181-3C>T rs1411160897
NM_004637.6(RAB7A):c.277C>T (p.Pro93Ser) rs11549756
NM_004637.6(RAB7A):c.311A>G (p.Asp104Gly)
NM_004637.6(RAB7A):c.351C>G (p.Asn117Lys)
NM_004637.6(RAB7A):c.377A>G (p.Lys126Arg) rs1933806941
NM_004637.6(RAB7A):c.403G>A (p.Ala135Thr) rs368804888
NM_004637.6(RAB7A):c.421G>A (p.Ala141Thr)
NM_004637.6(RAB7A):c.434G>A (p.Ser145Asn) rs2107616079
NM_004637.6(RAB7A):c.448C>A (p.Pro150Thr) rs1320514833
NM_004637.6(RAB7A):c.456T>G (p.Phe152Leu) rs1933833236
NM_004637.6(RAB7A):c.464G>A (p.Ser155Asn)
NM_004637.6(RAB7A):c.467C>G (p.Ala156Gly) rs2107616088
NM_004637.6(RAB7A):c.467C>T (p.Ala156Val)
NM_004637.6(RAB7A):c.489G>C (p.Glu163Asp)
NM_004637.6(RAB7A):c.528+2dup
NM_004637.6(RAB7A):c.54-15T>C rs748552184
NM_004637.6(RAB7A):c.74T>C (p.Met25Thr)
NM_004637.6(RAB7A):c.89A>G (p.Asn30Ser)

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