ClinVar Miner

List of variants in gene EHMT1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 41
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HGVS dbSNP
NM_024757.5(EHMT1):c.*17G>A rs886063744
NM_024757.5(EHMT1):c.*204C>T rs886063745
NM_024757.5(EHMT1):c.*551T>G rs886063746
NM_024757.5(EHMT1):c.*663G>A rs750578794
NM_024757.5(EHMT1):c.*870T>G rs756114316
NM_024757.5(EHMT1):c.1148C>T (p.Ser383Leu) rs771654748
NM_024757.5(EHMT1):c.1160G>A (p.Arg387His) rs776502547
NM_024757.5(EHMT1):c.1181A>C (p.Glu394Ala) rs773281152
NM_024757.5(EHMT1):c.1249-11T>C rs561072157
NM_024757.5(EHMT1):c.1299C>T (p.Thr433=) rs374367377
NM_024757.5(EHMT1):c.1360G>A (p.Gly454Ser) rs774046148
NM_024757.5(EHMT1):c.150G>A (p.Ala50=) rs371344592
NM_024757.5(EHMT1):c.1513G>A (p.Gly505Ser) rs757679895
NM_024757.5(EHMT1):c.153C>T (p.Asp51=) rs765396242
NM_024757.5(EHMT1):c.159G>T (p.Glu53Asp) rs202066668
NM_024757.5(EHMT1):c.183C>T (p.Ser61=) rs774448433
NM_024757.5(EHMT1):c.1931A>C (p.Lys644Thr) rs767536068
NM_024757.5(EHMT1):c.2142A>G (p.Gly714=) rs758845539
NM_024757.5(EHMT1):c.2167G>A (p.Ala723Thr) rs886063736
NM_024757.5(EHMT1):c.2175C>T (p.Ile725=) rs527754873
NM_024757.5(EHMT1):c.2192+11A>T rs759729046
NM_024757.5(EHMT1):c.2664C>T (p.Leu888=) rs200849773
NM_024757.5(EHMT1):c.2712+13C>T rs370446866
NM_024757.5(EHMT1):c.2882G>A (p.Arg961Gln) rs886063737
NM_024757.5(EHMT1):c.2922G>A (p.Thr974=) rs748716122
NM_024757.5(EHMT1):c.3035+3G>A rs765407306
NM_024757.5(EHMT1):c.3036G>C (p.Arg1012Ser) rs886063738
NM_024757.5(EHMT1):c.3107G>T (p.Ser1036Ile) rs369941047
NM_024757.5(EHMT1):c.3123C>G (p.Val1041=) rs141527497
NM_024757.5(EHMT1):c.3214A>G (p.Asn1072Asp) rs886063739
NM_024757.5(EHMT1):c.3258+14C>T rs886063740
NM_024757.5(EHMT1):c.3377C>T (p.Ala1126Val) rs560251933
NM_024757.5(EHMT1):c.3641T>C (p.Met1214Thr) rs781134719
NM_024757.5(EHMT1):c.3803C>G (p.Ala1268Gly) rs886063741
NM_024757.5(EHMT1):c.3834C>A (p.Ala1278=) rs886063742
NM_024757.5(EHMT1):c.3848A>C (p.Glu1283Ala) rs398124408
NM_024757.5(EHMT1):c.3894A>G (p.Leu1298=) rs886063743
NM_024757.5(EHMT1):c.405G>T (p.Gln135His) rs200982880
NM_024757.5(EHMT1):c.533C>A (p.Thr178Asn) rs777497639
NM_024757.5(EHMT1):c.551C>T (p.Ala184Val) rs886063735
NM_024757.5(EHMT1):c.575C>T (p.Pro192Leu) rs35285441

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