ClinVar Miner

List of variants in gene RAB23 studied for RAB23-related Carpenter syndrome

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_016277.5(RAB23):c.619G>A (p.Gly207Ser) rs1040461 0.11622
NM_016277.5(RAB23):c.301T>G (p.Ser101Ala) rs45479896 0.00575
NM_016277.5(RAB23):c.-23C>T rs145059995 0.00424
NM_016277.5(RAB23):c.*544G>A rs138311113 0.00213
NM_016277.5(RAB23):c.536A>C (p.Glu179Ala) rs150440590 0.00055
NM_016277.5(RAB23):c.434T>A (p.Leu145Ter) rs121908171 0.00037
NM_016277.5(RAB23):c.51T>C (p.Asn17=) rs141279756 0.00026
NM_016277.5(RAB23):c.552G>A (p.Thr184=) rs201731610 0.00016
NM_016277.5(RAB23):c.346A>G (p.Thr116Ala) rs138803099 0.00015
NM_016277.5(RAB23):c.25G>A (p.Ala9Thr) rs150655349 0.00013
NM_016277.5(RAB23):c.546A>C (p.Glu182Asp) rs377375386 0.00008
NM_016277.5(RAB23):c.93A>G (p.Lys31=) rs201735614 0.00007
NM_016277.5(RAB23):c.*145T>C rs189570356 0.00005
NM_016277.5(RAB23):c.123C>T (p.Thr41=) rs759408401 0.00005
NM_016277.5(RAB23):c.616T>A (p.Ser206Thr) rs202181599 0.00005
NM_016277.5(RAB23):c.90C>G (p.Cys30Trp) rs776515230 0.00005
NM_016277.5(RAB23):c.*618A>G rs886061653 0.00004
NM_016277.5(RAB23):c.*81G>T rs1304531152 0.00004
NM_016277.5(RAB23):c.171T>C (p.Asp57=) rs368714271 0.00004
NM_016277.5(RAB23):c.255T>C (p.Cys85=) rs374601145 0.00004
NM_016277.5(RAB23):c.481+10C>T rs546078370 0.00004
NM_016277.5(RAB23):c.534T>C (p.Ala178=) rs201820320 0.00004
NM_016277.5(RAB23):c.54A>G (p.Gly18=) rs767442221 0.00004
NM_016277.5(RAB23):c.670A>T (p.Thr224Ser) rs748638791 0.00004
NM_016277.5(RAB23):c.-49C>T rs45474592 0.00003
NM_016277.5(RAB23):c.218C>T (p.Ala73Val) rs556931606 0.00001
NM_016277.5(RAB23):c.222T>C (p.Ile74=) rs759497648 0.00001
NM_016277.5(RAB23):c.223A>T (p.Thr75Ser) rs774195943 0.00001
NM_016277.5(RAB23):c.239G>A (p.Arg80Gln) rs145669565 0.00001
NM_016277.5(RAB23):c.398+9G>A rs376839366 0.00001
NM_016277.5(RAB23):c.399-14A>T rs974936952 0.00001
NM_016277.5(RAB23):c.408dup (p.Glu137Ter) rs1438138090 0.00001
NM_016277.5(RAB23):c.48G>C (p.Gly16=) rs1454253077 0.00001
NM_016277.5(RAB23):c.714A>G (p.Ter238=) rs142290596 0.00001
NM_016277.5(RAB23):c.82C>T (p.Arg28Ter) rs765443042 0.00001
NM_016277.5(RAB23):c.*117A>G rs1764790940
NM_016277.5(RAB23):c.-66+5021dup rs1286074062
NM_016277.5(RAB23):c.156-9T>C rs1380069219
NM_016277.5(RAB23):c.208del (p.Glu70fs)
NM_016277.5(RAB23):c.315_316del (p.Lys106fs)
NM_016277.5(RAB23):c.389G>C (p.Cys130Ser) rs1485030118
NM_016277.5(RAB23):c.394A>T (p.Lys132Ter)
NM_016277.5(RAB23):c.398+1G>A rs2127998616
NM_016277.5(RAB23):c.399-2A>G
NM_016277.5(RAB23):c.416T>C (p.Leu139Pro) rs1593208594
NM_016277.5(RAB23):c.551C>T (p.Thr184Met) rs140295281
NM_016277.5(RAB23):c.559del (p.Ser187fs) rs2127997645
NM_016277.5(RAB23):c.664C>G (p.Gln222Glu) rs756536052
NM_016277.5(RAB23):c.664_667del (p.Gln222fs)
NM_016277.5(RAB23):c.701G>C (p.Cys234Ser)
NM_016277.5(RAB23):c.712T>G (p.Ter238Glu) rs751619487
NM_016277.5(RAB23):c.86dup (p.Tyr29Ter) rs1593223800

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