ClinVar Miner

List of variants in gene MMAA reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_172250.3(MMAA):c.*1227A>T rs375194713
NM_172250.3(MMAA):c.*1284G>A rs564976817
NM_172250.3(MMAA):c.*1584A>G rs530538534
NM_172250.3(MMAA):c.*1610C>T rs185925141
NM_172250.3(MMAA):c.*1779T>C rs886059097
NM_172250.3(MMAA):c.*177A>G rs572996882
NM_172250.3(MMAA):c.*1782A>G rs114134771
NM_172250.3(MMAA):c.*1838G>A rs886059098
NM_172250.3(MMAA):c.*188A>G rs886059091
NM_172250.3(MMAA):c.*1897_*1901del rs377206435
NM_172250.3(MMAA):c.*1918G>A rs755382235
NM_172250.3(MMAA):c.*1924T>C rs886059100
NM_172250.3(MMAA):c.*192G>A rs188845060
NM_172250.3(MMAA):c.*1952T>C rs79927727
NM_172250.3(MMAA):c.*1988A>T rs141116337
NM_172250.3(MMAA):c.*2019A>G rs886059102
NM_172250.3(MMAA):c.*229T>C rs886059092
NM_172250.3(MMAA):c.*2343A>G rs886059103
NM_172250.3(MMAA):c.*2364A>G rs13129907
NM_172250.3(MMAA):c.*2378A>G rs886059104
NM_172250.3(MMAA):c.*2445A>C rs886059105
NM_172250.3(MMAA):c.*2471G>A rs886059106
NM_172250.3(MMAA):c.*2479G>A rs886059107
NM_172250.3(MMAA):c.*2617C>A rs886059108
NM_172250.3(MMAA):c.*2627A>G rs886059109
NM_172250.3(MMAA):c.*2807C>T rs7675466
NM_172250.3(MMAA):c.*2808G>A rs543019315
NM_172250.3(MMAA):c.*2903C>T rs886059110
NM_172250.3(MMAA):c.*3035A>C rs576544645
NM_172250.3(MMAA):c.*3125C>T rs886059111
NM_172250.3(MMAA):c.*3222T>C rs886059112
NM_172250.3(MMAA):c.*3254A>C rs539831571
NM_172250.3(MMAA):c.*3257del rs886059113
NM_172250.3(MMAA):c.*3285G>A rs142885287
NM_172250.3(MMAA):c.*3356del rs577478683
NM_172250.3(MMAA):c.*342A>G rs886059093
NM_172250.3(MMAA):c.*3801A>G rs886059116
NM_172250.3(MMAA):c.*4103G>A rs191381122
NM_172250.3(MMAA):c.*4228T>C rs533826043
NM_172250.3(MMAA):c.*4533C>T rs114762906
NM_172250.3(MMAA):c.*540A>T rs886059094
NM_172250.3(MMAA):c.*541A>G rs114729477
NM_172250.3(MMAA):c.*589C>G rs886059095
NM_172250.3(MMAA):c.*600G>A rs112882351
NM_172250.3(MMAA):c.*67G>A rs886059090
NM_172250.3(MMAA):c.*703C>T rs548243828
NM_172250.3(MMAA):c.*890G>A rs771012374
NM_172250.3(MMAA):c.*942A>G rs886059096
NM_172250.3(MMAA):c.-66+10G>C rs546775043
NM_172250.3(MMAA):c.-68C>T rs886059087
NM_172250.3(MMAA):c.-69G>T rs886059086
NM_172250.3(MMAA):c.1078C>T (p.Arg360Trp) rs6812252
NM_172250.3(MMAA):c.1121G>A (p.Ser374Asn) rs778178659
NM_172250.3(MMAA):c.1177G>A (p.Glu393Lys) rs144313458
NM_172250.3(MMAA):c.1193T>C (p.Ile398Thr) rs777459994
NM_172250.3(MMAA):c.124C>G (p.Gln42Glu) rs758345818
NM_172250.3(MMAA):c.128C>T (p.Pro43Leu) rs886059088
NM_172250.3(MMAA):c.383T>C (p.Leu128Pro) rs560188002
NM_172250.3(MMAA):c.597G>A (p.Glu199=) rs116773849
NM_172250.3(MMAA):c.630A>G (p.Pro210=) rs374347679
NM_172250.3(MMAA):c.862G>A (p.Val288Ile) rs886059089
NM_172250.3(MMAA):c.904A>T (p.Ile302Leu) rs369128670
NM_172250.3(MMAA):c.912G>A (p.Ala304=) rs371769807
NM_172250.3(MMAA):c.977G>A (p.Arg326His) rs201547892

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