ClinVar Miner

List of variants in gene AIP reported as uncertain significance by GeneDx

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_003977.4(AIP):c.68G>A (p.Gly23Glu) rs116940576 0.00115
NM_003977.4(AIP):c.911G>A (p.Arg304Gln) rs104894190 0.00115
NM_003977.4(AIP):c.301G>A (p.Val101Met) rs147931650 0.00085
NM_003977.4(AIP):c.26G>A (p.Arg9Gln) rs139459091 0.00037
NM_003977.4(AIP):c.517G>A (p.Glu173Lys) rs138902236 0.00034
NM_003977.4(AIP):c.733G>A (p.Glu245Lys) rs150645662 0.00012
NM_003977.4(AIP):c.973C>T (p.Arg325Trp) rs765927395 0.00010
NM_003977.4(AIP):c.827C>T (p.Ala276Val) rs61741147 0.00009
NM_003977.4(AIP):c.561C>T (p.Asn187=) rs142037029 0.00008
NM_003977.4(AIP):c.724C>G (p.Leu242Val) rs772782309 0.00008
NM_003977.4(AIP):c.572G>A (p.Arg191His) rs141826817 0.00007
NM_003977.4(AIP):c.403C>T (p.His135Tyr) rs150487522 0.00006
NM_003977.4(AIP):c.967C>T (p.Arg323Trp) rs188965257 0.00006
NM_003977.4(AIP):c.940C>T (p.Arg314Trp) rs375740557 0.00005
NM_003977.4(AIP):c.692C>T (p.Thr231Met) rs532170807 0.00004
NM_003977.4(AIP):c.562C>T (p.Arg188Trp) rs577617733 0.00003
NM_003977.4(AIP):c.619G>A (p.Ala207Thr) rs1323279729 0.00002
NM_003977.4(AIP):c.919C>T (p.Arg307Trp) rs758248161 0.00002
NM_003977.4(AIP):c.334A>G (p.Lys112Glu) rs1489145468 0.00001
NM_003977.4(AIP):c.6G>A (p.Ala2=) rs1865725846 0.00001
NM_003977.4(AIP):c.745G>A (p.Glu249Lys) rs1313811815 0.00001
NM_003977.4(AIP):c.783C>T (p.Tyr261=) rs267606576 0.00001
NM_003977.4(AIP):c.874C>G (p.Leu292Val) rs764465139 0.00001
NM_003977.4(AIP):c.913G>A (p.Glu305Lys) rs923956036 0.00001
NM_003977.4(AIP):c.944A>C (p.Gln315Pro) rs886048585 0.00001
NM_003977.4(AIP):c.-2G>A
NM_003977.4(AIP):c.25C>T (p.Arg9Trp) rs1057523115
NM_003977.4(AIP):c.308A>G (p.Lys103Arg) rs267606548
NM_003977.4(AIP):c.341C>A (p.Pro114His) rs1865849163
NM_003977.4(AIP):c.427C>G (p.Gln143Glu)
NM_003977.4(AIP):c.533C>T (p.Ala178Val) rs763723045
NM_003977.4(AIP):c.645+2T>C rs1293512916
NM_003977.4(AIP):c.676C>G (p.Leu226Val)
NM_003977.4(AIP):c.685C>G (p.Gln229Glu) rs1400972107
NM_003977.4(AIP):c.790_792del (p.Asn264del) rs760690172
NM_003977.4(AIP):c.830C>T (p.Ala277Val)
NM_003977.4(AIP):c.845A>G (p.Gln282Arg) rs2134256527
NM_003977.4(AIP):c.899C>T (p.Pro300Leu) rs2134256678

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