ClinVar Miner

List of variants in gene IGHMBP2 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 88
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HGVS dbSNP
NM_002180.2(IGHMBP2):c.*117G>A rs745828352
NM_002180.2(IGHMBP2):c.*255T>C rs564244
NM_002180.2(IGHMBP2):c.*415G>A rs886048609
NM_002180.2(IGHMBP2):c.*417C>A rs117542830
NM_002180.2(IGHMBP2):c.*425G>A rs144205786
NM_002180.2(IGHMBP2):c.*427C>T rs3750980
NM_002180.2(IGHMBP2):c.*466G>A rs542162905
NM_002180.2(IGHMBP2):c.*648G>A rs139118510
NM_002180.2(IGHMBP2):c.*648G>T rs139118510
NM_002180.2(IGHMBP2):c.*665C>T rs9769
NM_002180.2(IGHMBP2):c.*681T>C rs9095
NM_002180.2(IGHMBP2):c.*692A>G rs188469352
NM_002180.2(IGHMBP2):c.*6C>T rs117995705
NM_002180.2(IGHMBP2):c.*744G>A rs116625875
NM_002180.2(IGHMBP2):c.*788C>T rs886048610
NM_002180.2(IGHMBP2):c.-28C>A rs117368938
NM_002180.2(IGHMBP2):c.-2C>T rs4930624
NM_002180.2(IGHMBP2):c.-4G>A rs752980392
NM_002180.2(IGHMBP2):c.-68T>C rs57258566
NM_002180.2(IGHMBP2):c.1015C>T (p.Leu339Phe) rs149045005
NM_002180.2(IGHMBP2):c.103A>G (p.Ile35Val) rs199586231
NM_002180.2(IGHMBP2):c.1060+8G>T rs201147313
NM_002180.2(IGHMBP2):c.1104C>T (p.Tyr368=) rs148157556
NM_002180.2(IGHMBP2):c.1125C>T (p.Asp375=) rs140296831
NM_002180.2(IGHMBP2):c.1193C>T (p.Ala398Val) rs35193202
NM_002180.2(IGHMBP2):c.1194G>A (p.Ala398=) rs745534850
NM_002180.2(IGHMBP2):c.1290C>T (p.Tyr430=) rs140654955
NM_002180.2(IGHMBP2):c.1340C>G (p.Ala447Gly) rs144240271
NM_002180.2(IGHMBP2):c.1422C>A (p.Asp474Glu) rs61731907
NM_002180.2(IGHMBP2):c.1478C>T (p.Thr493Ile) rs780594709
NM_002180.2(IGHMBP2):c.151C>G (p.Gln51Glu) rs117061430
NM_002180.2(IGHMBP2):c.1538-8C>G rs115320302
NM_002180.2(IGHMBP2):c.1554C>T (p.Val518=) rs11228413
NM_002180.2(IGHMBP2):c.1587T>G (p.Gly529=) rs886048604
NM_002180.2(IGHMBP2):c.180C>T (p.Tyr60=) rs34617762
NM_002180.2(IGHMBP2):c.1827G>A (p.Ala609=) rs541245852
NM_002180.2(IGHMBP2):c.1874C>T (p.Thr625Ile) rs886048605
NM_002180.2(IGHMBP2):c.1939G>A (p.Val647Ile) rs77822399
NM_002180.2(IGHMBP2):c.2011A>G (p.Thr671Ala) rs622082
NM_002180.2(IGHMBP2):c.2040G>A (p.Gln680=) rs886048606
NM_002180.2(IGHMBP2):c.2080C>T (p.Arg694Trp) rs2236654
NM_002180.2(IGHMBP2):c.2194A>G (p.Met732Val) rs750717921
NM_002180.2(IGHMBP2):c.2224A>G (p.Met742Val) rs754473710
NM_002180.2(IGHMBP2):c.222C>A (p.Ser74=) rs139237340
NM_002180.2(IGHMBP2):c.2316C>T (p.Ser772=) rs546382
NM_002180.2(IGHMBP2):c.2322A>G (p.Glu774=) rs11228414
NM_002180.2(IGHMBP2):c.2355G>A (p.Arg785=) rs147954772
NM_002180.2(IGHMBP2):c.2360C>T (p.Pro787Leu) rs141594765
NM_002180.2(IGHMBP2):c.2361G>A (p.Pro787=) rs187924099
NM_002180.2(IGHMBP2):c.2439G>A (p.Ala813=) rs624147
NM_002180.2(IGHMBP2):c.2467C>T (p.Arg823Cys) rs192806153
NM_002180.2(IGHMBP2):c.2532G>A (p.Ala844=) rs2228207
NM_002180.2(IGHMBP2):c.2532G>T (p.Ala844=) rs2228207
NM_002180.2(IGHMBP2):c.256+9G>A rs118015540
NM_002180.2(IGHMBP2):c.2612-15G>A rs372230504
NM_002180.2(IGHMBP2):c.2636C>A (p.Thr879Lys) rs17612126
NM_002180.2(IGHMBP2):c.2646C>A (p.Asp882Glu) rs372629862
NM_002180.2(IGHMBP2):c.2674A>G (p.Lys892Glu) rs201970407
NM_002180.2(IGHMBP2):c.2683A>G (p.Asn895Asp) rs886048607
NM_002180.2(IGHMBP2):c.2753G>A (p.Arg918His) rs368584364
NM_002180.2(IGHMBP2):c.2755C>A (p.Arg919Ser) rs145945230
NM_002180.2(IGHMBP2):c.2782G>A (p.Glu928Lys) rs2275996
NM_002180.2(IGHMBP2):c.2787C>G (p.Ile929Met) rs761854167
NM_002180.2(IGHMBP2):c.2793C>T (p.Gly931=) rs139926138
NM_002180.2(IGHMBP2):c.2837G>A (p.Arg946Gln) rs149824485
NM_002180.2(IGHMBP2):c.2856C>T (p.Ala952=) rs759627672
NM_002180.2(IGHMBP2):c.2872A>G (p.Asn958Asp) rs141873613
NM_002180.2(IGHMBP2):c.2883G>A (p.Leu961=) rs3750977
NM_002180.2(IGHMBP2):c.2922T>G (p.Asp974Glu) rs147674615
NM_002180.2(IGHMBP2):c.2975G>A (p.Gly992Glu) rs886048608
NM_002180.2(IGHMBP2):c.2979G>A (p.Thr993=) rs201760315
NM_002180.2(IGHMBP2):c.366C>T (p.His122=) rs144401213
NM_002180.2(IGHMBP2):c.381C>G (p.Ser127Arg) rs775782198
NM_002180.2(IGHMBP2):c.547+9T>G rs886048603
NM_002180.2(IGHMBP2):c.548-10T>G rs139207271
NM_002180.2(IGHMBP2):c.57T>C (p.Leu19=) rs1249463
NM_002180.2(IGHMBP2):c.602T>C (p.Leu201Ser) rs560096
NM_002180.2(IGHMBP2):c.696G>T (p.Val232=) rs748899869
NM_002180.2(IGHMBP2):c.714T>C (p.Val238=) rs755582766
NM_002180.2(IGHMBP2):c.726C>A (p.Ala242=) rs76690064
NM_002180.2(IGHMBP2):c.726C>G (p.Ala242=) rs76690064
NM_002180.2(IGHMBP2):c.741C>T (p.Ala247=) rs76707931
NM_002180.2(IGHMBP2):c.767C>G (p.Ala256Gly) rs148095551
NM_002180.2(IGHMBP2):c.823A>G (p.Ile275Val) rs10896380
NM_002180.2(IGHMBP2):c.857G>A (p.Arg286Gln) rs200566598
NM_002180.2(IGHMBP2):c.901G>A (p.Asp301Asn) rs139635469
NM_002180.2(IGHMBP2):c.912+4G>A rs758392980
NM_002180.2(IGHMBP2):c.963T>C (p.Asn321=) rs771900045

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