ClinVar Miner

List of variants in gene ALAD reported as uncertain significance for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000031.6(ALAD):c.*363G>A rs576008526 0.00175
NM_000031.6(ALAD):c.*400G>A rs557867804 0.00110
NM_000031.6(ALAD):c.*1464A>G rs559359572 0.00053
NM_000031.6(ALAD):c.715-14C>A rs201135240 0.00041
NM_000031.6(ALAD):c.*422G>T rs41276805 0.00038
NM_000031.6(ALAD):c.-75-11A>G rs187909805 0.00024
NM_000031.6(ALAD):c.29G>C (p.Gly10Ala) rs199655229 0.00022
NM_000031.6(ALAD):c.874G>A (p.Gly292Arg) rs200781693 0.00021
NM_000031.6(ALAD):c.*1832T>C rs903858525 0.00019
NM_000031.6(ALAD):c.277G>A (p.Ala93Thr) rs138313868 0.00019
NM_000031.6(ALAD):c.724G>A (p.Val242Ile) rs200180791 0.00016
NM_000031.6(ALAD):c.678G>T (p.Leu226=) rs190497588 0.00015
NM_000031.6(ALAD):c.264C>T (p.Asp88=) rs377534006 0.00012
NM_000031.6(ALAD):c.940A>G (p.Ile314Val) rs557510313 0.00011
NM_000031.6(ALAD):c.770A>G (p.Tyr257Cys) rs769181980 0.00010
NM_000031.6(ALAD):c.784C>T (p.Arg262Trp) rs777485356 0.00010
NM_000031.6(ALAD):c.16G>A (p.Val6Ile) rs766501537 0.00006
NM_000031.6(ALAD):c.439C>T (p.Arg147Cys) rs777664535 0.00006
NM_000031.6(ALAD):c.501G>A (p.Pro167=) rs376714503 0.00006
NM_000031.6(ALAD):c.870G>A (p.Gln290=) rs759917153 0.00005
NM_000031.6(ALAD):c.*643G>T rs182766085 0.00004
NM_000031.6(ALAD):c.-70G>T rs774433320 0.00004
NM_000031.6(ALAD):c.241G>A (p.Val81Ile) rs200963049 0.00004
NM_000031.6(ALAD):c.801+14C>T rs369933664 0.00004
NM_000031.6(ALAD):c.*381G>A rs886063363 0.00003
NM_000031.6(ALAD):c.-76+15G>T rs756965057 0.00003
NM_000031.6(ALAD):c.*127C>T rs561104906 0.00002
NM_000031.6(ALAD):c.*498C>T rs1025631016 0.00002
NM_000031.6(ALAD):c.715G>A (p.Asp239Asn) rs752186527 0.00002
NM_000031.6(ALAD):c.*1511T>C rs745513769 0.00001
NM_000031.6(ALAD):c.*1631G>A rs886063359 0.00001
NM_000031.6(ALAD):c.474C>G (p.Ala158=) rs1340298448 0.00001
NM_000031.6(ALAD):c.521G>A (p.Arg174His) rs750462706 0.00001
NM_000031.6(ALAD):c.897C>T (p.Ala299=) rs370242589 0.00001
NM_000031.6(ALAD):c.*1007G>A rs8177823
NM_000031.6(ALAD):c.*106C>G rs8177820
NM_000031.6(ALAD):c.*1280G>A rs190137021
NM_000031.6(ALAD):c.*1280G>C rs190137021
NM_000031.6(ALAD):c.*12C>T rs1827462434
NM_000031.6(ALAD):c.*1322G>A rs11789221
NM_000031.6(ALAD):c.*1470G>A rs886063360
NM_000031.6(ALAD):c.*1671A>T rs1827403039
NM_000031.6(ALAD):c.*1675C>T rs756771103
NM_000031.6(ALAD):c.*1741G>A rs886063358
NM_000031.6(ALAD):c.*1787A>C rs1588080129
NM_000031.6(ALAD):c.*1804T>C rs1327333635
NM_000031.6(ALAD):c.*1864A>C rs886063357
NM_000031.6(ALAD):c.*1915del rs886063356
NM_000031.6(ALAD):c.*234G>A rs1023159630
NM_000031.6(ALAD):c.*438G>C rs886063362
NM_000031.6(ALAD):c.*459_*463del rs886063361
NM_000031.6(ALAD):c.*676dup rs532401659
NM_000031.6(ALAD):c.*760T>C rs1827430851
NM_000031.6(ALAD):c.*920C>T rs1827424865
NM_000031.6(ALAD):c.1A>G (p.Met1Val) rs752500552
NM_000031.6(ALAD):c.415G>A (p.Gly139Arg)
NM_000031.6(ALAD):c.446G>A (p.Arg149Gln) rs528493383
NM_000031.6(ALAD):c.520C>T (p.Arg174Cys) rs758622234
NM_000031.6(ALAD):c.910A>G (p.Met304Val) rs1588081960
NM_000031.6(ALAD):c.931+15G>A rs886063364

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