ClinVar Miner

List of variants in gene SETD2 reported as not provided by ITMI

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_014159.7(SETD2):c.5885C>T (p.Pro1962Leu) rs4082155 0.49386
NM_014159.7(SETD2):c.3240G>A (p.Met1080Ile) rs76208147 0.02797
NM_014159.7(SETD2):c.2704G>C (p.Glu902Gln) rs58906143 0.01669
NM_014159.7(SETD2):c.2543C>T (p.Ala848Val) rs75248784 0.00870
NM_014159.7(SETD2):c.557C>T (p.Pro186Leu) rs78759480 0.00723
NM_014159.7(SETD2):c.2783C>G (p.Thr928Arg) rs72895708 0.00228
NM_014159.7(SETD2):c.2302G>C (p.Val768Leu) rs9311404 0.00182
NM_014159.7(SETD2):c.3229A>G (p.Thr1077Ala) rs114719990 0.00095
NM_014159.7(SETD2):c.1775C>A (p.Thr592Lys) rs115569620 0.00088
NM_014159.7(SETD2):c.3097A>G (p.Thr1033Ala) rs145759179 0.00063
NM_014159.7(SETD2):c.2251C>A (p.Pro751Thr) rs115788094 0.00034
NM_014159.7(SETD2):c.1579A>G (p.Ile527Val) rs373069098 0.00033
NM_014159.7(SETD2):c.4193T>C (p.Ile1398Thr) rs145732065 0.00032
NM_014159.7(SETD2):c.5900G>A (p.Gly1967Asp) rs143991928 0.00031
NM_014159.7(SETD2):c.2450T>C (p.Met817Thr) rs115023083 0.00026
NM_014159.7(SETD2):c.5812G>A (p.Val1938Ile) rs116417406 0.00024
NM_014159.7(SETD2):c.4839+278C>T rs587777970 0.00019
NM_014159.7(SETD2):c.2794G>A (p.Val932Ile) rs141532143 0.00010
NM_014159.7(SETD2):c.4839+332G>T rs587777969 0.00009
NM_014159.7(SETD2):c.2283G>A (p.Met761Ile) rs188887061 0.00007
NM_014159.7(SETD2):c.1343G>A (p.Arg448Gln) rs564020755 0.00006
NM_014159.7(SETD2):c.4262T>C (p.Leu1421Pro) rs587778677 0.00006
NM_014159.7(SETD2):c.2155A>G (p.Asn719Asp) rs115859828 0.00005
NM_014159.7(SETD2):c.310C>A (p.Pro104Thr) rs539506462 0.00004
NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly) rs201752182 0.00003
NM_014159.7(SETD2):c.784A>C (p.Ser262Arg) rs544730198 0.00003
NM_014159.7(SETD2):c.3136A>G (p.Asn1046Asp) rs199890800 0.00002
NM_014159.7(SETD2):c.1687A>G (p.Ile563Val) rs587778668 0.00001
NM_014159.7(SETD2):c.2297T>C (p.Met766Thr) rs587778675 0.00001
NM_014159.7(SETD2):c.2632G>C (p.Gly878Arg) rs587778671 0.00001
NM_014159.7(SETD2):c.2713T>C (p.Ser905Pro) rs587778676 0.00001
NM_014159.7(SETD2):c.3131G>A (p.Ser1044Asn) rs587778673 0.00001
NM_014159.7(SETD2):c.5633T>C (p.Phe1878Ser) rs587778665 0.00001
NM_014159.7(SETD2):c.5945A>G (p.Asp1982Gly) rs587778664 0.00001
NM_014159.7(SETD2):c.6269G>A (p.Arg2090Gln) rs149758106 0.00001
NM_014159.7(SETD2):c.6664C>T (p.Pro2222Ser) rs587778666 0.00001
NM_014159.7(SETD2):c.7352C>T (p.Ala2451Val) rs587778667 0.00001
NM_014159.7(SETD2):c.2275A>G (p.Lys759Glu) rs200479097
NM_014159.7(SETD2):c.227G>C (p.Ser76Thr) rs587778670
NM_014159.7(SETD2):c.2575A>T (p.Thr859Ser) rs587778669
NM_014159.7(SETD2):c.2824G>A (p.Gly942Arg) rs587778672
NM_014159.7(SETD2):c.3142G>A (p.Glu1048Lys) rs587778674
NM_014159.7(SETD2):c.4526G>A (p.Arg1509Lys) rs528393799
NM_014159.7(SETD2):c.4972T>G (p.Ser1658Ala) rs587778678
NM_014159.7(SETD2):c.5369G>C (p.Arg1790Pro) rs376246790

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